Showing entry for Serine/threonine-protein kinase B-raf


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT008075
Protein NameSerine/threonine-protein kinase B-raf
Uniport IdP15056
GeneBRAF
Gene Id673
DomainC1_1; Pkinase_Tyr; RBD
Pfam PF00130   PF07714   PF02196  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
6. Human Diseases 6.12 Drug resistance: Antineoplastic hsa01521 EGFR tyrosine kinase inhibitor resistance
6. Human Diseases 6.12 Drug resistance: Antineoplastic hsa01522 Endocrine resistance
3. Environmental Information Processing 3.2 Signal transduction hsa04010 MAPK signaling pathway
3. Environmental Information Processing 3.2 Signal transduction hsa04012 ErbB signaling pathway
3. Environmental Information Processing 3.2 Signal transduction hsa04015 Rap1 signaling pathway
3. Environmental Information Processing 3.2 Signal transduction hsa04024 cAMP signaling pathway
5. Organismal Systems 5.1 Immune system hsa04062 Chemokine signaling pathway
3. Environmental Information Processing 3.2 Signal transduction hsa04068 FoxO signaling pathway
3. Environmental Information Processing 3.2 Signal transduction hsa04150 mTOR signaling pathway
5. Organismal Systems 5.3 Circulatory system hsa04270 Vascular smooth muscle contraction
4. Cellular Processes 4.3 Cellular community - eukaryotes hsa04510 Focal adhesion
5. Organismal Systems 5.1 Immune system hsa04650 Natural killer cell mediated cytotoxicity
5. Organismal Systems 5.6 Nervous system hsa04720 Long-term potentiation
5. Organismal Systems 5.6 Nervous system hsa04722 Neurotrophin signaling pathway
5. Organismal Systems 5.6 Nervous system hsa04726 Serotonergic synapse
5. Organismal Systems 5.6 Nervous system hsa04730 Long-term depression
4. Cellular Processes 4.5 Cell motility hsa04810 Regulation of actin cytoskeleton
5. Organismal Systems 5.2 Endocrine system hsa04910 Insulin signaling pathway
5. Organismal Systems 5.2 Endocrine system hsa04914 Progesterone-mediated oocyte maturation
5. Organismal Systems 5.2 Endocrine system hsa04928 Parathyroid hormone synthesis, secretion and action
6. Human Diseases 6.7 Endocrine and metabolic diseases hsa04934 Cushing syndrome
6. Human Diseases 6.5 Substance dependence hsa05034 Alcoholism
6. Human Diseases 6.9 Infectious diseases: Viral hsa05160 Hepatitis C
6. Human Diseases 6.9 Infectious diseases: Viral hsa05161 Hepatitis B
6. Human Diseases 6.1 Cancers: Overview hsa05200 Pathways in cancer
6. Human Diseases 6.1 Cancers: Overview hsa05205 Proteoglycans in cancer
6. Human Diseases 6.2 Cancers: Specific types hsa05210 Colorectal cancer
6. Human Diseases 6.2 Cancers: Specific types hsa05211 Renal cell carcinoma
6. Human Diseases 6.2 Cancers: Specific types hsa05212 Pancreatic cancer
6. Human Diseases 6.2 Cancers: Specific types hsa05213 Endometrial cancer
6. Human Diseases 6.2 Cancers: Specific types hsa05214 Glioma
6. Human Diseases 6.2 Cancers: Specific types hsa05215 Prostate cancer
6. Human Diseases 6.2 Cancers: Specific types hsa05216 Thyroid cancer
6. Human Diseases 6.2 Cancers: Specific types hsa05218 Melanoma
6. Human Diseases 6.2 Cancers: Specific types hsa05219 Bladder cancer
6. Human Diseases 6.2 Cancers: Specific types hsa05220 Chronic myeloid leukemia
6. Human Diseases 6.2 Cancers: Specific types hsa05221 Acute myeloid leukemia
6. Human Diseases 6.2 Cancers: Specific types hsa05223 Non-small cell lung cancer
6. Human Diseases 6.2 Cancers: Specific types hsa05224 Breast cancer
6. Human Diseases 6.2 Cancers: Specific types hsa05225 Hepatocellular carcinoma
6. Human Diseases 6.2 Cancers: Specific types hsa05226 Gastric cancer
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0000186 activation of MAPKK activity
Biological Process GO:0009887 animal organ morphogenesis
Biological Process GO:0071277 cellular response to calcium ion
Biological Process GO:0007173 epidermal growth factor receptor signaling pathway
Biological Process GO:0090150 establishment of protein localization to membrane
Biological Process GO:0000165 MAPK cascade
Biological Process GO:0043066 negative regulation of apoptotic process
Biological Process GO:0070374 positive regulation of ERK1 and ERK2 cascade
Biological Process GO:0010628 positive regulation of gene expression
Biological Process GO:0010828 positive regulation of glucose transmembrane transport
Biological Process GO:0033138 positive regulation of peptidyl-serine phosphorylation
Biological Process GO:0006468 protein phosphorylation
Biological Process GO:0070413 trehalose metabolism in response to stress
molecular function GO:0005524 ATP binding
molecular function GO:0005509 calcium ion binding
molecular function GO:0042802 identical protein binding
molecular function GO:0004672 protein kinase activity
molecular function GO:0004674 protein serine/threonine kinase activity
molecular function GO:0097110 scaffold protein binding
cellular component GO:0005829 cytosol
cellular component GO:0043231 intracellular membrane-bounded organelle
cellular component GO:0005634 nucleus
cellular component GO:0005886 plasma membrane
Reactome
Pathway Id Pathway Name
R-HSA-1280215 Cytokine Signaling in Immune system
R-HSA-1295596 Spry regulation of FGF signaling
R-HSA-162582 Signal Transduction
R-HSA-162582 Signal Transduction
R-HSA-1643685 Disease
R-HSA-166520 Signaling by NTRKs
R-HSA-166520 Signaling by NTRKs
R-HSA-168256 Immune System
R-HSA-169893 Prolonged ERK activation events
R-HSA-169893 Prolonged ERK activation events
R-HSA-170968 Frs2-mediated activation
R-HSA-170968 Frs2-mediated activation
R-HSA-170984 ARMS-mediated activation
R-HSA-187037 Signaling by NTRK1 (TRKA)
R-HSA-187037 Signaling by NTRK1 (TRKA)
R-HSA-187687 Signalling to ERKs
R-HSA-187687 Signalling to ERKs
R-HSA-187706 Signalling to p38 via RIT and RIN
R-HSA-190236 Signaling by FGFR
R-HSA-5654726 Negative regulation of FGFR1 signaling
R-HSA-5654727 Negative regulation of FGFR2 signaling
R-HSA-5654732 Negative regulation of FGFR3 signaling
R-HSA-5654733 Negative regulation of FGFR4 signaling
R-HSA-5654736 Signaling by FGFR1
R-HSA-5654738 Signaling by FGFR2
R-HSA-5654741 Signaling by FGFR3
R-HSA-5654743 Signaling by FGFR4
R-HSA-5663202 Diseases of signal transduction by growth factor receptors and second messengers
R-HSA-5673000 RAF activation
R-HSA-5673001 RAF/MAP kinase cascade
R-HSA-5674135 MAP2K and MAPK activation
R-HSA-5674499 Negative feedback regulation of MAPK pathway
R-HSA-5675221 Negative regulation of MAPK pathway
R-HSA-5683057 MAPK family signaling cascades
R-HSA-5684996 MAPK1/MAPK3 signaling
R-HSA-6802946 Signaling by moderate kinase activity BRAF mutants
R-HSA-6802948 Signaling by high-kinase activity BRAF mutants
R-HSA-6802949 Signaling by RAS mutants
R-HSA-6802952 Signaling by BRAF and RAF fusions
R-HSA-6802955 Paradoxical activation of RAF signaling by kinase inactive BRAF
R-HSA-6802957 Oncogenic MAPK signaling
R-HSA-9006934 Signaling by Receptor Tyrosine Kinases
R-HSA-9006934 Signaling by Receptor Tyrosine Kinases
R-HSA-9607240 FLT3 Signaling
R-HSA-9649948 Signaling downstream of RAS mutants
R-HSA-9656223 Signaling by RAF1 mutants
R-HSA-9660537 Signaling by MRAS-complex mutants
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000768 BXGD000007 Congenital Abnormality Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0000772 BXGD000009 Multiple congenital anomalies Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0001206 BXGD000033 Acromegaly Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
C0001418 BXGD000050 Adenocarcinoma Neoplasms
C0001430 BXGD000054 Adenoma Neoplasms
C0001546 BXGD000060 Adjustment Disorders Mental Disorders
C0002170 BXGD000105 Alopecia Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0002448 BXGD000115 Ameloblastoma Neoplasms
C0002792 BXGD000129 anaphylaxis Immune System Diseases
C0002793 BXGD000130 Anaplasia Pathological Conditions, Signs and Symptoms; Neoplasms
C0003175 BXGD000187 Anthrax disease Infections
C0003463 BXGD000192 Anus Neoplasms Digestive System Diseases; Neoplasms
C0003492 BXGD000198 Aortic coarctation Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0003811 BXGD000222 Cardiac Arrhythmia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0003857 BXGD000228 Congenital arteriovenous malformation Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0003862 BXGD000230 Arthralgia Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases
C0003864 BXGD000231 Arthritis Musculoskeletal Diseases
C0003872 BXGD000235 Arthritis, Psoriatic Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0003873 BXGD000236 Rheumatoid Arthritis Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
C0004045 BXGD000249 Asphyxia Neonatorum Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0004114 BXGD000255 Astrocytoma Neoplasms
C0004135 BXGD000257 Ataxia Telangiectasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
C0004364 BXGD000270 Autoimmune Diseases Immune System Diseases
C0004565 BXGD000276 Melanoma, B16 Neoplasms
C0005684 BXGD000319 Malignant neoplasm of urinary bladder Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0005695 BXGD000323 Bladder Neoplasm Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0005745 BXGD000331 Blepharoptosis Eye Diseases
C0006118 BXGD000372 Brain Neoplasms Neoplasms; Nervous System Diseases
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006281 BXGD000388 Congenital bronchogenic cyst Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Respiratory Tract Diseases
C0006384 BXGD000395 Bundle-Branch Block Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0006413 BXGD000397 Burkitt Lymphoma Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases
C0006625 BXGD000401 Cachexia Pathological Conditions, Signs and Symptoms
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007095 BXGD000423 Carcinoid Tumor Neoplasms
C0007097 BXGD000424 Carcinoma Neoplasms
C0007102 BXGD000425 Malignant tumor of colon Digestive System Diseases; Neoplasms
C0007103 BXGD000426 Malignant neoplasm of endometrium Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0007112 BXGD000429 Adenocarcinoma of prostate Neoplasms; Male Urogenital Diseases
C0007113 BXGD000430 Rectal Carcinoma Digestive System Diseases; Neoplasms
C0007114 BXGD000431 Malignant neoplasm of skin Neoplasms; Skin and Connective Tissue Diseases
C0007115 BXGD000432 Malignant neoplasm of thyroid Neoplasms; Endocrine System Diseases
C0007120 BXGD000435 Bronchioloalveolar Adenocarcinoma Neoplasms
C0007129 BXGD000439 Merkel cell carcinoma Neoplasms; Infections
C0007130 BXGD000440 Mucinous Adenocarcinoma Neoplasms
C0007131 BXGD000441 Non-Small Cell Lung Carcinoma Neoplasms; Respiratory Tract Diseases
C0007133 BXGD000442 Carcinoma, Papillary Neoplasms
C0007134 BXGD000443 Renal Cell Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0007137 BXGD000445 Squamous cell carcinoma Neoplasms
C0007140 BXGD000447 Carcinosarcoma Neoplasms
C0007194 BXGD000452 Hypertrophic Cardiomyopathy Cardiovascular Diseases
C0007682 BXGD000471 CNS disorder Nervous System Diseases
C0007762 BXGD000477 Cerebellar Neoplasms Neoplasms; Nervous System Diseases
C0008073 BXGD000518 Developmental Disabilities Mental Disorders
C0008309 BXGD000525 Bile duct adenoma Neoplasms
C0008487 BXGD000545 Chordoma Neoplasms
C0008497 BXGD000549 Choriocarcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0008626 BXGD000559 Congenital chromosomal disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0009075 BXGD000579 Melanoma, Cloudman S91 Neoplasms
C0009241 BXGD000595 Cognition Disorders Mental Disorders
C0009319 BXGD000596 Colitis Digestive System Diseases
C0009324 BXGD000597 Ulcerative Colitis Digestive System Diseases
C0009375 BXGD000602 Colonic Neoplasms Digestive System Diseases; Neoplasms
C0009376 BXGD000603 Colonic Polyps Pathological Conditions, Signs and Symptoms
C0009402 BXGD000605 Colorectal Carcinoma Digestive System Diseases; Neoplasms
C0009404 BXGD000606 Colorectal Neoplasms Digestive System Diseases; Neoplasms
C0009405 BXGD000607 Hereditary Nonpolyposis Colorectal Neoplasms Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases
C0009421 BXGD000608 Comatose Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0009681 BXGD000621 Anomalous pulmonary artery Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
C0009761 BXGD000627 Conjunctival Neoplasms Neoplasms; Eye Diseases
C0009806 BXGD000633 Constipation Pathological Conditions, Signs and Symptoms
C0010276 BXGD000659 Craniopharyngioma Neoplasms
C0010346 BXGD000664 Crohn Disease Digestive System Diseases
C0010417 BXGD000670 Cryptorchidism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases
C0010633 BXGD000679 Cystadenoma Neoplasms
C0010635 BXGD000680 Cystadenoma, Mucinous Neoplasms
C0010823 BXGD000690 Cytomegalovirus Infections Infections
C0011168 BXGD000700 Deglutition Disorders Digestive System Diseases; Otorhinolaryngologic Diseases
C0011603 BXGD000734 Dermatitis Skin and Connective Tissue Diseases
C0011615 BXGD000738 Dermatitis, Atopic Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases
C0011649 BXGD000746 Dermoid Cyst Neoplasms
C0011854 BXGD000753 Diabetes Mellitus, Insulin-Dependent Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases
C0011860 BXGD000755 Diabetes Mellitus, Non-Insulin-Dependent Nutritional and Metabolic Diseases; Endocrine System Diseases
C0011991 BXGD000766 Diarrhea Pathological Conditions, Signs and Symptoms
C0012739 BXGD000786 Disseminated Intravascular Coagulation Hemic and Lymphatic Diseases
C0013274 BXGD000809 Patent ductus arteriosus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0013336 BXGD000815 Dwarfism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0013362 BXGD000817 Dysarthria Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0013403 BXGD000832 Dysplastic Nevus Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C0014116 BXGD000892 Endocardial Cushion Defects Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0014170 BXGD000902 Endometrial Neoplasms Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0014175 BXGD000904 Endometriosis Female Urogenital Diseases and Pregnancy Complications
C0014457 BXGD000915 Eosinophilia Hemic and Lymphatic Diseases
C0014474 BXGD000917 Ependymoma Neoplasms
C0014511 BXGD000920 Epithelial cyst Neoplasms
C0014544 BXGD000926 Epilepsy Nervous System Diseases
C0014547 BXGD000927 Epilepsies, Partial Nervous System Diseases
C0014743 BXGD000946 Erythema Nodosum Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders
C0014850 BXGD000957 Esophageal Atresia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
C0015230 BXGD000969 Exanthema Skin and Connective Tissue Diseases
C0015300 BXGD000973 Exophthalmos Eye Diseases
C0015414 BXGD000989 Eye Neoplasms Neoplasms; Eye Diseases
C0015519 BXGD000999 Factor X Deficiency Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0015526 BXGD001001 Factor XII Deficiency Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0015544 BXGD001003 Failure to Thrive Pathological Conditions, Signs and Symptoms
C0015672 BXGD001011 Fatigue Pathological Conditions, Signs and Symptoms
C0015934 BXGD001026 Fetal Growth Retardation Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
C0015967 BXGD001030 Fever Pathological Conditions, Signs and Symptoms
C0016045 BXGD001037 fibroma Neoplasms
C0016057 BXGD001042 Fibrosarcoma Neoplasms
C0016689 BXGD001073 Freckles Skin and Connective Tissue Diseases
C0016842 BXGD001083 Congenital pectus excavatum Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0017168 BXGD001101 Gastroesophageal reflux disease Digestive System Diseases
C0017416 BXGD001110 Genital Neoplasms, Female Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0017525 BXGD001112 Giant Cell Tumors Neoplasms
C0017636 BXGD001131 Glioblastoma Neoplasms
C0017638 BXGD001132 Glioma Neoplasms
C0017653 BXGD001135 Glomus Tumor Neoplasms
C0017658 BXGD001138 Glomerulonephritis Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0017925 BXGD001156 Glycogen Storage Disease Type VI Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0018021 BXGD001162 Goiter Endocrine System Diseases
C0018023 BXGD001164 Nodular Goiter Endocrine System Diseases
C0018202 BXGD001183 Granulomatous Angiitis Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
C0018552 BXGD001202 Hamartoma Neoplasms
C0018598 BXGD001207 Melanoma, Harding-Passey Neoplasms
C0018671 BXGD001211 Head and Neck Neoplasms Neoplasms
C0018681 BXGD001214 Headache Pathological Conditions, Signs and Symptoms
C0018784 BXGD001220 Sensorineural Hearing Loss (disorder) Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0018798 BXGD001223 Congenital Heart Defects Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0018799 BXGD001224 Heart Diseases Cardiovascular Diseases
C0018817 BXGD001235 Atrial Septal Defects Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0018818 BXGD001236 Ventricular Septal Defects Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0018920 BXGD001246 Hemangioma, Cavernous Neoplasms; Hemic and Lymphatic Diseases; Cardiovascular Diseases
C0018923 BXGD001248 Hemangiosarcoma Neoplasms
C0018932 BXGD001251 Hematochezia Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0019202 BXGD001302 Hepatolenticular Degeneration Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Nutritional and Metabolic Diseases; Nervous System Diseases
C0019209 BXGD001305 Hepatomegaly Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0019618 BXGD001339 Histiocytosis Hemic and Lymphatic Diseases
C0019621 BXGD001340 Histiocytosis, Langerhans-Cell Respiratory Tract Diseases; Hemic and Lymphatic Diseases
C0019623 BXGD001341 Malignant histiocytosis Neoplasms; Hemic and Lymphatic Diseases
C0019624 BXGD001342 Histiocytosis, Non-Langerhans-Cell Hemic and Lymphatic Diseases
C0019625 BXGD001343 Sinus histiocytosis Hemic and Lymphatic Diseases
C0019829 BXGD001350 Hodgkin Disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0020224 BXGD001366 Polyhydramnios Female Urogenital Diseases and Pregnancy Complications
C0020255 BXGD001369 Hydrocephalus Nervous System Diseases
C0020295 BXGD001372 Hydronephrosis Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0020437 BXGD001381 Hypercalcemia Nutritional and Metabolic Diseases
C0020505 BXGD001412 Hyperphagia Pathological Conditions, Signs and Symptoms
C0020534 BXGD001421 Orbital separation excessive Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0020538 BXGD001422 Hypertensive disease Cardiovascular Diseases
C0020625 BXGD001451 Hyponatremia Nutritional and Metabolic Diseases
C0020676 BXGD001462 Hypothyroidism Endocrine System Diseases
C0020757 BXGD001466 Ichthyoses Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0020981 BXGD001474 Angioimmunoblastic Lymphadenopathy Immune System Diseases; Hemic and Lymphatic Diseases
C0021051 BXGD001475 Immunologic Deficiency Syndromes Immune System Diseases
C0021364 BXGD001500 Male infertility Male Urogenital Diseases
C0021390 BXGD001503 Inflammatory Bowel Diseases Digestive System Diseases
C0021432 BXGD001505 Infratentorial Neoplasms Neoplasms; Nervous System Diseases
C0021670 BXGD001509 insulinoma Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0022572 BXGD001553 keratoacanthoma Skin and Connective Tissue Diseases
C0022593 BXGD001560 Keratosis Skin and Connective Tissue Diseases
C0022602 BXGD001564 Actinic keratosis Neoplasms; Skin and Connective Tissue Diseases
C0022658 BXGD001570 Kidney Diseases Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022660 BXGD001571 Kidney Failure, Acute Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022665 BXGD001573 Kidney Neoplasm Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022672 BXGD001574 Acute Kidney Tubular Necrosis Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0023381 BXGD001641 Letterer-Siwe Disease Respiratory Tract Diseases; Hemic and Lymphatic Diseases
C0023418 BXGD001642 leukemia Neoplasms
C0023434 BXGD001643 Chronic Lymphocytic Leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0023443 BXGD001648 Hairy Cell Leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0023449 BXGD001650 Acute lymphocytic leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0023452 BXGD001651 Childhood Acute Lymphoblastic Leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0023465 BXGD001656 Acute monocytic leukemia Neoplasms
C0023467 BXGD001658 Leukemia, Myelocytic, Acute Neoplasms
C0023473 BXGD001661 Myeloid Leukemia, Chronic Neoplasms; Hemic and Lymphatic Diseases
C0023480 BXGD001664 Leukemia, Myelomonocytic, Chronic Neoplasms; Hemic and Lymphatic Diseases
C0023484 BXGD001666 Leukemia, Plasma Cell Neoplasms; Immune System Diseases
C0023486 BXGD001668 Prolymphocytic Leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0023487 BXGD001669 Acute Promyelocytic Leukemia Neoplasms
C0023501 BXGD001674 Leukemoid Reaction Hemic and Lymphatic Diseases
C0023518 BXGD001677 Leukocytosis Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases
C0023530 BXGD001683 Leukopenia Hemic and Lymphatic Diseases
C0023903 BXGD001720 Liver neoplasms Digestive System Diseases; Neoplasms
C0024115 BXGD001732 Lung diseases Respiratory Tract Diseases
C0024121 BXGD001735 Lung Neoplasms Neoplasms; Respiratory Tract Diseases
C0024232 BXGD001751 Lymphatic Metastasis Pathological Conditions, Signs and Symptoms; Neoplasms
C0024236 BXGD001752 Lymphedema Hemic and Lymphatic Diseases
C0024291 BXGD001757 Lymphohistiocytosis, Hemophagocytic Hemic and Lymphatic Diseases
C0024299 BXGD001758 Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0024301 BXGD001759 Lymphoma, Follicular Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0024302 BXGD001760 Reticulosarcoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0024305 BXGD001763 Lymphoma, Non-Hodgkin Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0024312 BXGD001766 Lymphopenia Immune System Diseases; Hemic and Lymphatic Diseases
C0024314 BXGD001767 Lymphoproliferative Disorders Immune System Diseases; Hemic and Lymphatic Diseases
C0024419 BXGD001769 Waldenstrom Macroglobulinemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
C0024433 BXGD001771 Macrostomia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C0024623 BXGD001791 Malignant neoplasm of stomach Digestive System Diseases; Neoplasms
C0024636 BXGD001793 Malocclusion Stomatognathic Diseases
C0024694 BXGD001797 Mandibular Neoplasms Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
C0024796 BXGD001806 Marfan Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
C0024814 BXGD001809 Marinesco-Sjogren syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0025149 BXGD001826 Medulloblastoma Neoplasms
C0025202 BXGD001832 melanoma Neoplasms
C0025205 BXGD001833 Melanoma, Experimental Neoplasms
C0025209 BXGD001834 Melanosis Skin and Connective Tissue Diseases
C0025286 BXGD001850 Meningioma Neoplasms; Nervous System Diseases
C0025362 BXGD001866 Mental Retardation Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0025500 BXGD001874 Mesothelioma Neoplasms
C0025990 BXGD001884 Micrognathism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
C0026010 BXGD001886 Microphthalmos Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0026106 BXGD001889 Mild Mental Retardation Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C0026267 BXGD001896 Mitral Valve Prolapse Syndrome Cardiovascular Diseases
C0026277 BXGD001899 Mixed Salivary Gland Tumor Neoplasms
C0026499 BXGD001905 Monosomy Pathological Conditions, Signs and Symptoms
C0026650 BXGD001913 Movement Disorders Nervous System Diseases
C0026764 BXGD001928 Multiple Myeloma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
C0026826 BXGD001935 Muscle Hypertonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0026827 BXGD001936 Muscle hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0026985 BXGD001956 Myelodysplasia
C0027051 BXGD001963 Myocardial Infarction Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0027092 BXGD001971 Myopia Eye Diseases
C0027430 BXGD001988 Nasal Polyps Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases
C0027498 BXGD001994 Nausea and vomiting Pathological Conditions, Signs and Symptoms
C0027533 BXGD001995 Neck Neoplasms Neoplasms
C0027627 BXGD002006 Neoplasm Metastasis Pathological Conditions, Signs and Symptoms; Neoplasms
C0027651 BXGD002009 Neoplasms Neoplasms
C0027659 BXGD002012 Neoplasms, Experimental Neoplasms
C0027666 BXGD002018 Neoplasms, Radiation-Induced Neoplasms; Wounds and Injuries
C0027672 BXGD002020 Neoplastic Syndromes, Hereditary Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C0027697 BXGD002022 Nephritis Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0027707 BXGD002024 Nephritis, Interstitial Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0027708 BXGD002025 Nephroblastoma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0027726 BXGD002030 Nephrotic Syndrome Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0027766 BXGD002034 Nervous System Neoplasms Neoplasms; Nervous System Diseases
C0027809 BXGD002040 Neurilemmoma Neoplasms
C0027819 BXGD002043 Neuroblastoma Neoplasms
C0027830 BXGD002046 neurofibroma Neoplasms; Nervous System Diseases
C0027831 BXGD002047 Neurofibromatosis 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C0027859 BXGD002052 Acoustic Neuroma Neoplasms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0027947 BXGD002061 Neutropenia Hemic and Lymphatic Diseases
C0027960 BXGD002062 Nevus Neoplasms
C0027962 BXGD002064 Melanocytic nevus Neoplasms
C0028259 BXGD002073 Nodule
C0028326 BXGD002075 Noonan Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
C0028738 BXGD002081 Nystagmus Eye Diseases; Nervous System Diseases
C0028754 BXGD002082 Obesity Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0028880 BXGD002097 Odontogenic Tumors Neoplasms
C0028945 BXGD002099 oligodendroglioma Neoplasms
C0029124 BXGD002113 Optic Atrophy Eye Diseases; Nervous System Diseases
C0029166 BXGD002119 Oral Manifestations Pathological Conditions, Signs and Symptoms; Stomatognathic Diseases
C0029182 BXGD002121 orbit (eye disorders) Eye Diseases
C0029295 BXGD002129 Oropharyngeal Neoplasms Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C0029453 BXGD002154 Osteopenia Nutritional and Metabolic Diseases; Musculoskeletal Diseases
C0029463 BXGD002160 Osteosarcoma Neoplasms
C0029925 BXGD002181 Ovarian Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0030283 BXGD002200 Pancreatic Cyst Digestive System Diseases; Neoplasms
C0030297 BXGD002204 Pancreatic Neoplasm Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0030305 BXGD002206 Pancreatitis Digestive System Diseases
C0030326 BXGD002209 Panniculitis Skin and Connective Tissue Diseases
C0030353 BXGD002213 Papilledema Eye Diseases; Nervous System Diseases
C0030354 BXGD002214 Papilloma Neoplasms
C0030421 BXGD002218 Paraganglioma Neoplasms
C0030567 BXGD002240 Parkinson Disease Nervous System Diseases
C0031117 BXGD002285 Peripheral Neuropathy Nervous System Diseases
C0031511 BXGD002304 Pheochromocytoma Neoplasms
C0031941 BXGD002317 Pineal Gland Neoplasm Neoplasms; Nervous System Diseases
C0032019 BXGD002321 Pituitary Neoplasms Neoplasms; Nervous System Diseases; Endocrine System Diseases
C0032131 BXGD002330 Plasmacytoma Neoplasms; Immune System Diseases
C0032580 BXGD002362 Adenomatous Polyposis Coli Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C0032584 BXGD002363 polyps Pathological Conditions, Signs and Symptoms
C0032897 BXGD002378 Prader-Willi Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
C0032927 BXGD002381 Precancerous Conditions Neoplasms
C0033036 BXGD002389 Atrial Premature Complexes Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0033377 BXGD002406 Ptosis Pathological Conditions, Signs and Symptoms
C0033578 BXGD002408 Prostatic Neoplasms Neoplasms; Male Urogenital Diseases
C0033626 BXGD002412 Protein Deficiency Nutritional and Metabolic Diseases
C0034012 BXGD002449 Delayed Puberty Endocrine System Diseases
C0034089 BXGD002462 Pulmonary Valve Stenosis Cardiovascular Diseases
C0034885 BXGD002490 Rectal Neoplasms Digestive System Diseases; Neoplasms
C0035290 BXGD002525 Reticulohistiocytic granuloma Hemic and Lymphatic Diseases
C0035309 BXGD002530 Retinal Diseases Eye Diseases
C0035335 BXGD002540 Retinoblastoma Neoplasms; Eye Diseases
C0035412 BXGD002548 Rhabdomyosarcoma Neoplasms
C0036095 BXGD002576 Salivary Gland Neoplasms Neoplasms; Stomatognathic Diseases
C0036202 BXGD002581 Sarcoidosis Hemic and Lymphatic Diseases
C0036439 BXGD002615 Scoliosis, unspecified Musculoskeletal Diseases
C0036572 BXGD002625 Seizures Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0036631 BXGD002626 Seminoma Neoplasms
C0036920 BXGD002645 Sezary Syndrome Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0037274 BXGD002676 Dermatologic disorders Skin and Connective Tissue Diseases
C0037277 BXGD002677 Skin Diseases, Genetic Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0037284 BXGD002679 Skin lesion Skin and Connective Tissue Diseases
C0037285 BXGD002680 Skin Manifestations Pathological Conditions, Signs and Symptoms
C0037286 BXGD002681 Skin Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C0037287 BXGD002682 Skin nodule Neoplasms; Skin and Connective Tissue Diseases
C0037315 BXGD002687 Sleep Apnea Syndromes Respiratory Tract Diseases; Nervous System Diseases
C0037579 BXGD002694 Soft Tissue Neoplasms Neoplasms
C0038002 BXGD002723 Splenomegaly Pathological Conditions, Signs and Symptoms
C0038356 BXGD002747 Stomach Neoplasms Digestive System Diseases; Neoplasms
C0038379 BXGD002752 Strabismus Eye Diseases; Nervous System Diseases
C0038478 BXGD002764 Struma Ovarii Neoplasms
C0038874 BXGD002783 Supratentorial Neoplasms Neoplasms; Nervous System Diseases
C0039103 BXGD002791 Synovitis Musculoskeletal Diseases
C0039445 BXGD002810 Hereditary hemorrhagic telangiectasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases
C0039538 BXGD002819 Teratoma Neoplasms
C0039685 BXGD002825 Tetralogy of Fallot Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0040100 BXGD002840 Thymoma Neoplasms; Hemic and Lymphatic Diseases
C0040128 BXGD002844 Thyroid Diseases Endocrine System Diseases
C0040136 BXGD002845 Thyroid Neoplasm Neoplasms; Endocrine System Diseases
C0040137 BXGD002846 Thyroid Nodule Neoplasms; Endocrine System Diseases
C0040147 BXGD002847 Thyroiditis Endocrine System Diseases
C0041341 BXGD002918 Tuberous Sclerosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C0041349 BXGD002920 Nephritis, Tubulointerstitial Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0041409 BXGD002924 Turner Syndrome, Male Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
C0042164 BXGD002965 Uveitis Eye Diseases
C0042571 BXGD002991 Vertigo Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0042834 BXGD003004 Vital capacity
C0042900 BXGD003012 Vitiligo Skin and Connective Tissue Diseases
C0042963 BXGD003018 Vomiting Pathological Conditions, Signs and Symptoms
C0043324 BXGD003040 Juvenile Xanthogranuloma Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
C0043346 BXGD003043 Xeroderma Pigmentosum Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0078918 BXGD003055 Albinism, Oculocutaneous Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases
C0079218 BXGD003066 Fibromatosis, Aggressive Neoplasms
C0079588 BXGD003084 Ichthyosis, X-Linked Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0079731 BXGD003087 B-Cell Lymphomas Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0079741 BXGD003089 Lymphoma, Intermediate-Grade Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0079744 BXGD003090 Diffuse Large B-Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0079745 BXGD003091 Lymphoma, Large-Cell, Follicular Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0079773 BXGD003100 Lymphoma, T-Cell, Cutaneous Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0080032 BXGD003105 Pleural Effusion, Malignant Neoplasms; Respiratory Tract Diseases
C0080174 BXGD003106 Spina Bifida Occulta Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0080218 BXGD003109 Tethered Cord Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0085074 BXGD003116 Granuloma Annulare Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0085136 BXGD003131 Central Nervous System Neoplasms Neoplasms; Nervous System Diseases
C0085281 BXGD003152 Addictive Behavior Behavior and Behavior Mechanisms
C0085584 BXGD003195 Encephalopathies Nervous System Diseases
C0085653 BXGD003225 Pyogenic granuloma Pathological Conditions, Signs and Symptoms
C0085669 BXGD003233 Acute leukemia Pathological Conditions, Signs and Symptoms; Neoplasms
C0086437 BXGD003282 Joint laxity Musculoskeletal Diseases
C0086692 BXGD003306 Benign Neoplasm Neoplasms
C0149722 BXGD003350 Hutchinson's Melanotic Freckle Neoplasms
C0149782 BXGD003365 Squamous cell carcinoma of lung Neoplasms; Respiratory Tract Diseases
C0149925 BXGD003387 Small cell carcinoma of lung Neoplasms; Respiratory Tract Diseases
C0149978 BXGD003397 Adenocarcinoma of rectum Digestive System Diseases; Neoplasms
C0151468 BXGD003424 Thyroid Gland Follicular Adenoma Neoplasms; Endocrine System Diseases
C0151526 BXGD003432 Premature Birth Female Urogenital Diseases and Pregnancy Complications
C0151546 BXGD003437 Oral Cavity Carcinoma Digestive System Diseases; Neoplasms; Stomatognathic Diseases
C0151611 BXGD003447 Electroencephalogram abnormal Nervous System Diseases
C0151718 BXGD003464 Hypocholesterolemia Nutritional and Metabolic Diseases
C0151740 BXGD003468 Intracranial Hypertension Nervous System Diseases
C0151779 BXGD003473 Cutaneous Melanoma Neoplasms; Skin and Connective Tissue Diseases
C0151786 BXGD003475 Muscle Weakness Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases
C0151811 BXGD003478 Subcutaneous nodule Neoplasms; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0151908 BXGD003502 Dry skin Skin and Connective Tissue Diseases
C0152013 BXGD003516 Adenocarcinoma of lung (disorder) Neoplasms
C0152021 BXGD003520 Congenital heart disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0152421 BXGD003586 Macrotia
C0152438 BXGD003592 Sprengel deformity Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0153381 BXGD003626 Malignant neoplasm of mouth Neoplasms; Stomatognathic Diseases
C0153446 BXGD003646 Malignant neoplasm of anus Digestive System Diseases; Neoplasms
C0153452 BXGD003647 Malignant neoplasm of gallbladder Digestive System Diseases; Neoplasms
C0153574 BXGD003667 Malignant Uterine Corpus Neoplasm Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0153594 BXGD003669 Malignant neoplasm of testis Neoplasms; Male Urogenital Diseases; Endocrine System Diseases
C0153633 BXGD003674 Malignant neoplasm of brain Neoplasms; Nervous System Diseases
C0153676 BXGD003679 Secondary malignant neoplasm of lung Neoplasms; Respiratory Tract Diseases
C0153687 BXGD003683 Secondary malignant neoplasm of skin Neoplasms; Skin and Connective Tissue Diseases
C0153690 BXGD003684 Secondary malignant neoplasm of bone Pathological Conditions, Signs and Symptoms; Neoplasms; Musculoskeletal Diseases
C0153943 BXGD003689 Benign neoplasm of stomach Digestive System Diseases; Neoplasms
C0154060 BXGD003697 Carcinoma in situ of stomach Digestive System Diseases; Neoplasms
C0156147 BXGD003838 Crohn's disease of large bowel Digestive System Diseases
C0158465 BXGD003887 Acquired cubitus valgus
C0158570 BXGD003892 Vascular anomaly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0158731 BXGD003902 Congenital pectus carinatum Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0158761 BXGD003905 Radioulnar Synostosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0162316 BXGD003936 Iron deficiency anemia Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
C0162323 BXGD003937 Polyarthritis Musculoskeletal Diseases
C0162504 BXGD003945 Neutrophilic Eccrine Hidradenitis Skin and Connective Tissue Diseases
C0162678 BXGD003974 Neurofibromatoses Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C0162830 BXGD003987 Dermatitis, Phototoxic Skin and Connective Tissue Diseases
C0162834 BXGD003988 Hyperpigmentation Skin and Connective Tissue Diseases
C0162848 BXGD003992 Lichenoid Eruptions Skin and Connective Tissue Diseases
C0175704 BXGD004010 LEOPARD Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
C0178874 BXGD004037 Tumor Progression Pathological Conditions, Signs and Symptoms
C0205647 BXGD004099 Follicular adenoma Neoplasms
C0205695 BXGD004106 Carcinoid, Goblet Cell Neoplasms
C0205696 BXGD004107 Anaplastic carcinoma Neoplasms
C0205698 BXGD004109 Undifferentiated carcinoma Neoplasms
C0205748 BXGD004117 Dysplastic Nevus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C0205768 BXGD004119 Subependymal Giant Cell Astrocytoma Neoplasms
C0205824 BXGD004128 Liposarcoma, Dedifferentiated Neoplasms
C0205851 BXGD004132 Germ cell tumor Neoplasms
C0205945 BXGD004142 Sarcoma, Spindle Cell Neoplasms
C0206180 BXGD004170 Ki-1+ Anaplastic Large Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0206620 BXGD004187 Lymphangioma, Cystic Neoplasms
C0206633 BXGD004198 Angiomyolipoma Neoplasms
C0206638 BXGD004203 Giant Cell Tumor of Bone Neoplasms
C0206651 BXGD004215 Clear Cell Sarcoma of Soft Tissue Neoplasms
C0206659 BXGD004222 Embryonal Carcinoma Neoplasms
C0206667 BXGD004228 Adrenal Cortical Adenoma Neoplasms; Endocrine System Diseases
C0206674 BXGD004232 Adenoma, Villous Neoplasms
C0206682 BXGD004237 Follicular thyroid carcinoma Neoplasms
C0206683 BXGD004238 Papillary and follicular adenocarcinoma Neoplasms
C0206685 BXGD004240 Acinar Cell Carcinoma Neoplasms
C0206686 BXGD004241 Adrenocortical carcinoma Neoplasms; Endocrine System Diseases
C0206687 BXGD004242 Carcinoma, Endometrioid Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0206693 BXGD004244 Medullary carcinoma Neoplasms
C0206694 BXGD004245 Mucoepidermoid Carcinoma Neoplasms
C0206695 BXGD004246 Carcinoma, Neuroendocrine Neoplasms
C0206696 BXGD004247 Carcinoma, Signet Ring Cell Neoplasms
C0206698 BXGD004248 Cholangiocarcinoma Neoplasms
C0206701 BXGD004251 Cystadenocarcinoma, Serous Neoplasms
C0206709 BXGD004257 Cystadenoma, Serous Neoplasms
C0206715 BXGD004261 Neoplasms, Neuroepithelial Neoplasms
C0206716 BXGD004262 Ganglioglioma Neoplasms
C0206726 BXGD004271 gliosarcoma Neoplasms
C0206729 BXGD004274 Neurofibrosarcoma Neoplasms; Nervous System Diseases
C0206735 BXGD004280 Melanoma, Amelanotic Neoplasms
C0206736 BXGD004281 Nevus, Blue Neoplasms
C0206739 BXGD004283 Epithelioid and spindle cell nevus Neoplasms
C0206740 BXGD004284 Calcifying Odontogenic Cyst Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
C0206754 BXGD004289 Neuroendocrine Tumors Neoplasms
C0206769 BXGD004291 Nevi and Melanomas Neoplasms
C0220597 BXGD004292 Adult Hodgkin Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0220603 BXGD004293 Childhood Brain Neoplasm Neoplasms; Nervous System Diseases
C0220605 BXGD004294 Adult Non-Hodgkin Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0220611 BXGD004295 Childhood Rhabdomyosarcoma Neoplasms
C0220612 BXGD004296 Childhood Non-Hodgkin Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0220620 BXGD004299 Gastrointestinal Carcinoid Tumor Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0220630 BXGD004302 Adult Liver Carcinoma Digestive System Diseases; Neoplasms
C0220633 BXGD004303 Uveal melanoma Neoplasms; Eye Diseases
C0220641 BXGD004305 Lip and Oral Cavity Carcinoma Neoplasms; Stomatognathic Diseases
C0220644 BXGD004306 Childhood Hodgkin Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0220650 BXGD004310 Metastatic malignant neoplasm to brain Pathological Conditions, Signs and Symptoms; Neoplasms; Nervous System Diseases
C0220668 BXGD004317 Congenital contractural arachnodactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0221013 BXGD004363 Mastocytosis, Systemic Neoplasms; Immune System Diseases
C0221055 BXGD004382 Paramyotonia Congenita (disorder) Musculoskeletal Diseases; Nervous System Diseases
C0221184 BXGD004402 Bitemporal Hemianopia Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C0221217 BXGD004408 Neck webbing Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0221263 BXGD004427 Cafe-au-Lait Spots Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0221354 BXGD004446 Frontal bossing Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0221355 BXGD004447 Macrocephaly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C0221356 BXGD004448 Brachycephaly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0221357 BXGD004449 Brachydactyly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0221358 BXGD004450 Long narrow head
C0221391 BXGD004456 Melanosis coli Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases
C0221406 BXGD004459 Pituitary-dependent Cushing's disease Nervous System Diseases; Endocrine System Diseases
C0221505 BXGD004466 Lesion of brain
C0234166 BXGD004628 Hyperexplexia Nervous System Diseases
C0234894 BXGD004699 Dermatitis acneiform Skin and Connective Tissue Diseases
C0234979 BXGD004707 Dysdiadochokinesis Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0235031 BXGD004714 Neurologic Symptoms Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0235752 BXGD004766 Port-Wine Stain Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0235782 BXGD004769 Gallbladder Carcinoma Digestive System Diseases; Neoplasms
C0235974 BXGD004796 Pancreatic carcinoma Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0238198 BXGD004893 Gastrointestinal Stromal Tumors Digestive System Diseases; Neoplasms
C0238339 BXGD004914 Hereditary pancreatitis Digestive System Diseases
C0238348 BXGD004915 Squamous cell carcinoma of penis Neoplasms; Male Urogenital Diseases
C0238397 BXGD004923 Pulmonary artery stenosis Cardiovascular Diseases
C0238461 BXGD004936 Anaplastic thyroid carcinoma Neoplasms
C0238462 BXGD004937 Medullary carcinoma of thyroid Neoplasms; Endocrine System Diseases
C0238463 BXGD004938 Papillary thyroid carcinoma Neoplasms; Endocrine System Diseases
C0239234 BXGD004974 Low set ears
C0239676 BXGD004989 High forehead
C0239998 BXGD005012 Recurrent infections Pathological Conditions, Signs and Symptoms; Infections; Musculoskeletal Diseases
C0240379 BXGD005033 Open mouth (finding)
C0240543 BXGD005042 Bulbous nose
C0240635 BXGD005047 Byzanthine arch palate Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases
C0240953 BXGD005067 Winged scapula
C0241074 BXGD005078 Hyperextensible skin
C0241654 BXGD005104 Abnormal heart valve morphology Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0242379 BXGD005157 Malignant neoplasm of lung Neoplasms; Respiratory Tract Diseases
C0242510 BXGD005173 Drug usage Chemically-Induced Disorders; Mental Disorders
C0242596 BXGD005181 Neoplasm, Residual Pathological Conditions, Signs and Symptoms; Neoplasms
C0242647 BXGD005184 Mucosa-Associated Lymphoid Tissue Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0242994 BXGD005205 Hantavirus Infections Infections
C0243038 BXGD005211 Carcinoma, Lewis Lung Neoplasms
C0259781 BXGD005219 Compound nevus of skin Neoplasms
C0259783 BXGD005221 mixed gliomas Neoplasms
C0259786 BXGD005223 Rhabdoid meningioma Neoplasms; Nervous System Diseases
C0260037 BXGD005227 Multiple tumors Neoplasms
C0262444 BXGD005244 Abnormality of the dentition Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C0262584 BXGD005256 Carcinoma, Small Cell Neoplasms
C0263218 BXGD005281 Pyogenic granuloma of skin Pathological Conditions, Signs and Symptoms; Neoplasms; Infections; Skin and Connective Tissue Diseases
C0263383 BXGD005296 Keratosis pilaris Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0263490 BXGD005314 Brittle hair
C0265325 BXGD005516 Turcot syndrome (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nervous System Diseases
C0265610 BXGD005555 Clinodactyly of fingers Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0266061 BXGD005618 Open Bite Stomatognathic Diseases
C0267026 BXGD005727 Actinic cheilitis Stomatognathic Diseases
C0267561 BXGD005761 Perianal fistula Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases
C0268398 BXGD005933 Familial lichen amyloidosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0269106 BXGD006054 Endosalpingiosis Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
C0270685 BXGD006084 Cerebral calcification Nutritional and Metabolic Diseases; Nervous System Diseases
C0271270 BXGD006178 Oculovestibuloauditory syndrome Eye Diseases; Nervous System Diseases; Cardiovascular Diseases
C0271623 BXGD006222 Hypogonadotropic hypogonadism Endocrine System Diseases
C0277959 BXGD006487 Coarse hair
C0278480 BXGD006510 Stage III Colon Cancer Digestive System Diseases; Neoplasms
C0278484 BXGD006511 Malignant neoplasm of colon stage IV Digestive System Diseases; Neoplasms
C0278488 BXGD006515 Carcinoma breast stage IV
C0278510 BXGD006526 Childhood Medulloblastoma Neoplasms
C0278592 BXGD006544 Adult Angiosarcoma Neoplasms
C0278595 BXGD006545 Adult Fibrosarcoma Neoplasms
C0278600 BXGD006546 Childhood Brain Stem Glioma
C0278622 BXGD006551 Adult Malignant Peripheral Nerve Sheath Tumor Neoplasms; Nervous System Diseases
C0278652 BXGD006554 Childhood Craniopharyngioma Neoplasms
C0278701 BXGD006566 Gastric Adenocarcinoma Digestive System Diseases; Neoplasms
C0278764 BXGD006581 Adult Burkitt Lymphoma Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases
C0278803 BXGD006593 Adenocarcinoma of small intestine Digestive System Diseases; Neoplasms
C0278851 BXGD006603 Stage IV Thyroid Gland Papillary Carcinoma AJCC v7 Neoplasms; Endocrine System Diseases
C0278875 BXGD006606 Adult Craniopharyngioma Neoplasms
C0278876 BXGD006607 Adult Medulloblastoma Neoplasms
C0278878 BXGD006609 Adult Glioblastoma Neoplasms
C0278879 BXGD006610 Childhood Burkitt Lymphoma Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases
C0278880 BXGD006611 Stage I Cutaneous Melanoma AJCC v6
C0278881 BXGD006612 stage II melanoma
C0278882 BXGD006613 Stage III Cutaneous Melanoma AJCC v6
C0278883 BXGD006614 Metastatic melanoma Neoplasms
C0278884 BXGD006615 Melanoma recurrent Neoplasms; Skin and Connective Tissue Diseases
C0278987 BXGD006620 Metastatic non-small cell lung cancer Neoplasms
C0278996 BXGD006621 Malignant Head and Neck Neoplasm Neoplasms
C0279000 BXGD006622 Liver and Intrahepatic Biliary Tract Carcinoma Digestive System Diseases; Neoplasms
C0279014 BXGD006623 Childhood Germ Cell Tumor Neoplasms
C0279068 BXGD006624 Childhood Solid Neoplasm
C0279070 BXGD006625 Adult Oligodendroglioma Neoplasms
C0279550 BXGD006635 Adult Rhabdomyosarcoma Neoplasms
C0279557 BXGD006636 Adenosquamous cell lung cancer Neoplasms; Respiratory Tract Diseases
C0279626 BXGD006657 Squamous cell carcinoma of esophagus Digestive System Diseases; Neoplasms
C0279628 BXGD006659 Adenocarcinoma Of Esophagus Digestive System Diseases; Neoplasms
C0279637 BXGD006665 Anal carcinoma Digestive System Diseases; Neoplasms
C0279651 BXGD006674 Gallbladder adenocarcinoma Digestive System Diseases; Neoplasms
C0279663 BXGD006676 Serous cystadenocarcinoma ovary Neoplasms
C0279672 BXGD006678 Cervical Adenocarcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0279680 BXGD006680 Transitional cell carcinoma of bladder Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0279702 BXGD006685 Conventional (Clear Cell) Renal Cell Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0279987 BXGD006706 Childhood Malignant Peripheral Nerve Sheath Tumor Neoplasms; Nervous System Diseases
C0279988 BXGD006707 Childhood Angiosarcoma Neoplasms
C0280099 BXGD006712 Adult Solid Neoplasm
C0280100 BXGD006713 Solid Neoplasm Neoplasms
C0280302 BXGD006735 Squamous cell carcinoma of lip Neoplasms; Skin and Connective Tissue Diseases; Stomatognathic Diseases
C0280474 BXGD006748 Childhood Glioblastoma Neoplasms
C0280475 BXGD006749 Childhood Oligodendroglioma Neoplasms
C0280483 BXGD006750 Adult Anaplastic Astrocytoma Neoplasms
C0280781 BXGD006758 Adult Pilocytic Astrocytoma Neoplasms
C0280783 BXGD006759 Juvenile Pilocytic Astrocytoma Neoplasms
C0280785 BXGD006760 Diffuse Astrocytoma Neoplasms
C0281361 BXGD006774 Adenocarcinoma of pancreas Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0302142 BXGD006831 Deformity Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0302323 BXGD006839 Reticulohistiocytosis
C0311361 BXGD006880 Adenomatous goiter Neoplasms; Endocrine System Diseases
C0332563 BXGD006894 Papule Pathological Conditions, Signs and Symptoms
C0333516 BXGD006957 Tumor necrosis Pathological Conditions, Signs and Symptoms
C0333983 BXGD006975 Hyperplastic Polyp Pathological Conditions, Signs and Symptoms
C0334108 BXGD006994 Multiple polyps Pathological Conditions, Signs and Symptoms
C0334121 BXGD006996 Inflammatory Myofibroblastic Tumor Pathological Conditions, Signs and Symptoms
C0334230 BXGD007001 Malignant tumor, fusiform cell type Neoplasms
C0334277 BXGD007017 Adenocarcinoma, metastatic Neoplasms
C0334307 BXGD007029 Tubulovillous adenoma Neoplasms
C0334345 BXGD007037 Apocrine adenoma Neoplasms
C0334348 BXGD007040 Hidradenoma Papilliferum Neoplasms
C0334350 BXGD007041 Eccrine papillary adenoma Neoplasms; Skin and Connective Tissue Diseases
C0334355 BXGD007042 Serous cystadenoma, borderline malignancy Neoplasms
C0334359 BXGD007044 Papillary serous cystadenocarcinoma Neoplasms
C0334424 BXGD007064 Nodular melanoma Neoplasms; Skin and Connective Tissue Diseases
C0334431 BXGD007066 Melanocytoma
C0334438 BXGD007068 Superficial spreading malignant melanoma of skin Neoplasms; Skin and Connective Tissue Diseases
C0334439 BXGD007069 Malignant desmoplastic melanoma Neoplasms
C0334443 BXGD007070 Epithelioid Cell Melanoma Neoplasms
C0334444 BXGD007071 Spindle Cell Melanoma Neoplasms
C0334459 BXGD007074 Infantile fibrosarcoma Neoplasms
C0334509 BXGD007095 Clear cell sarcoma, of tendons and aponeuroses Neoplasms
C0334525 BXGD007103 Struma ovarii, malignant Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0334533 BXGD007105 Arteriovenous hemangioma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Cardiovascular Diseases
C0334576 BXGD007118 Gliomatosis cerebri Neoplasms
C0334579 BXGD007120 Anaplastic astrocytoma Neoplasms
C0334580 BXGD007121 Protoplasmic astrocytoma Neoplasms
C0334581 BXGD007122 Gemistocytic astrocytoma Neoplasms
C0334582 BXGD007123 Fibrillary Astrocytoma Neoplasms
C0334583 BXGD007124 Pilocytic Astrocytoma Neoplasms
C0334586 BXGD007126 Pleomorphic Xanthoastrocytoma Neoplasms
C0334587 BXGD007127 Astroblastoma Neoplasms
C0334588 BXGD007128 Giant Cell Glioblastoma Neoplasms
C0334607 BXGD007135 Psammomatous Meningioma Neoplasms; Nervous System Diseases
C0334633 BXGD007143 Malignant lymphoma - lymphoplasmacytic Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0334663 BXGD007149 Histiocytic sarcoma Neoplasms; Hemic and Lymphatic Diseases
C0338070 BXGD007165 Childhood Cerebral Astrocytoma Neoplasms
C0338106 BXGD007167 Adenocarcinoma of colon Digestive System Diseases; Neoplasms
C0338656 BXGD007211 Impaired cognition Mental Disorders
C0340279 BXGD007314 Ventricular hypertrophy Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0341038 BXGD007385 Jaw Keratocyst Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
C0342190 BXGD007440 C-cell hyperplasia of thyroid Pathological Conditions, Signs and Symptoms; Endocrine System Diseases
C0342199 BXGD007443 Iodine deficiency syndrome Endocrine System Diseases
C0342276 BXGD007449 Maturity onset diabetes mellitus in young Nutritional and Metabolic Diseases; Endocrine System Diseases
C0342409 BXGD007476 Hypophysitis Nervous System Diseases; Endocrine System Diseases
C0342422 BXGD007479 Pituitary gland enlarged Nervous System Diseases; Endocrine System Diseases
C0343641 BXGD007636 Human papilloma virus infection Infections
C0344460 BXGD007674 Carcinoma ex pleomorphic adenoma Neoplasms; Stomatognathic Diseases
C0344482 BXGD007678 Hypoplasia of corpus callosum Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0345392 BXGD007732 Congenital kyphoscoliosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0345904 BXGD007745 Malignant neoplasm of liver Digestive System Diseases; Neoplasms
C0345905 BXGD007746 Intrahepatic Cholangiocarcinoma Neoplasms
C0345946 BXGD007750 Squamous cell carcinoma of trachea Neoplasms
C0345964 BXGD007755 Adenoma of lung Neoplasms
C0346023 BXGD007765 Syringocystadenoma
C0346037 BXGD007768 Acral Lentiginous Malignant Melanoma Neoplasms; Skin and Connective Tissue Diseases
C0346040 BXGD007769 Stage 0 Skin Melanoma Neoplasms; Skin and Connective Tissue Diseases
C0346360 BXGD007815 Malignant melanoma of conjunctiva
C0346373 BXGD007817 Malignant melanoma of iris Neoplasms; Eye Diseases
C0346388 BXGD007819 Malignant melanoma of choroid Neoplasms; Eye Diseases
C0346398 BXGD007822 Mixed follicular and papillary thyroid carcinoma
C0346429 BXGD007828 Multiple malignancy Neoplasms
C0346627 BXGD007830 Intestinal Cancer Digestive System Diseases; Neoplasms
C0346647 BXGD007832 Malignant neoplasm of pancreas Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0346787 BXGD007834 Malignant melanoma of breast Neoplasms; Skin and Connective Tissue Diseases
C0346989 BXGD007841 Secondary malignant neoplasm of peritoneum
C0346990 BXGD007842 Carcinomatosis of peritoneal cavity Digestive System Diseases; Neoplasms
C0349515 BXGD007913 Amelanotic Skin Melanoma Neoplasms; Skin and Connective Tissue Diseases
C0349533 BXGD007918 Lymphoma of intestine Digestive System Diseases; Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0349534 BXGD007919 Carcinoma of anal margin Digestive System Diseases; Neoplasms
C0349588 BXGD007933 Short stature
C0349620 BXGD007936 Pilocytic astrocytoma of cerebellum Neoplasms; Nervous System Diseases
C0349632 BXGD007939 Splenic Marginal Zone B-Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0349633 BXGD007940 Hairy cell leukemia variant Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0349639 BXGD007943 Juvenile Myelomonocytic Leukemia Neoplasms; Hemic and Lymphatic Diseases
C0349658 BXGD007947 Trichoepithelioma Neoplasms
C0376338 BXGD007990 Diagnosis, Psychiatric Mental Disorders
C0376358 BXGD007992 Malignant neoplasm of prostate Neoplasms; Male Urogenital Diseases
C0376407 BXGD007996 Granulomatous Slack Skin Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0376545 BXGD008002 Hematologic Neoplasms Neoplasms; Hemic and Lymphatic Diseases
C0393525 BXGD008081 Progressive cerebellar ataxia Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0398597 BXGD008198 Histiocytic syndrome Immune System Diseases; Hemic and Lymphatic Diseases
C0398639 BXGD008208 Amegakaryocytic thrombocytopenia Hemic and Lymphatic Diseases
C0406484 BXGD008345 Sebaceous hyperplasia Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0406803 BXGD008373 Syringocystadenoma Papilliferum Neoplasms
C0423110 BXGD008471 Downward slant of palpebral fissure
C0423224 BXGD008475 Sunken eyes Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C0423798 BXGD008510 Increased tendency to bruise Wounds and Injuries
C0423867 BXGD008517 Fine hair
C0424295 BXGD008524 Hyperactive behavior Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0424605 BXGD008535 Developmental delay (disorder) Mental Disorders
C0431108 BXGD008657 Anaplastic Oligoastrocytoma Neoplasms
C0431112 BXGD008660 Anaplastic ganglioglioma Neoplasms
C0431128 BXGD008664 Papillary craniopharyngioma Neoplasms
C0431129 BXGD008665 Adamantinous Craniopharyngioma Neoplasms
C0431448 BXGD008691 Absent eyebrow Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0431478 BXGD008692 Posteriorly rotated ear
C0432072 BXGD008718 Dysmorphic features
C0432103 BXGD008722 Submucous cleft of hard palate Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C0432333 BXGD008778 Abnormal dermatoglyphic pattern Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0452138 BXGD008831 Sensorineural hearing loss, bilateral Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0457179 BXGD008885 Desmoplastic infantile astrocytoma Neoplasms
C0457521 BXGD008890 Unicystic ameloblastoma Neoplasms
C0474808 BXGD008959 Follicular neoplasm Neoplasms
C0475801 BXGD008971 Leukemia, Prolymphocytic, B-Cell Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0476089 BXGD008977 Endometrial Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0494165 BXGD009022 Secondary malignant neoplasm of liver Digestive System Diseases; Neoplasms
C0496905 BXGD009048 Neoplasm of uncertain or unknown behavior of stomach Digestive System Diseases; Neoplasms
C0496920 BXGD009049 Neoplasm of uncertain or unknown behavior of ovary Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0496956 BXGD009052 Neoplasm of uncertain or unknown behavior of breast Neoplasms; Skin and Connective Tissue Diseases
C0520739 BXGD009106 Hereditary pyropoikilocytosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases
C0520927 BXGD009124 Decreased fertility
C0521158 BXGD009130 Recurrent tumor
C0521525 BXGD009139 Short neck
C0521579 BXGD009144 Congenital strabismus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases
C0521585 BXGD009145 Gastrointestinal mucositis Digestive System Diseases; Stomatognathic Diseases
C0521698 BXGD009165 Vogt-Koyanagi-Harada like syndrome Eye Diseases
C0524620 BXGD009236 Metabolic Syndrome X Nutritional and Metabolic Diseases
C0524851 BXGD009246 Neurodegenerative Disorders Nervous System Diseases
C0541764 BXGD009259 Delayed bone age
C0544886 BXGD009319 Somatic mutation
C0546837 BXGD009343 Malignant neoplasm of esophagus Digestive System Diseases; Neoplasms
C0547065 BXGD009355 Mixed oligoastrocytoma Neoplasms
C0549410 BXGD009378 Palmar-plantar erythrodysesthesia syndrome Skin and Connective Tissue Diseases; Chemically-Induced Disorders
C0549473 BXGD009384 Thyroid carcinoma Neoplasms; Endocrine System Diseases
C0553694 BXGD009409 Oropharyngeal disorders Digestive System Diseases; Respiratory Tract Diseases; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C0553721 BXGD009415 Diminished sweating Skin and Connective Tissue Diseases; Nervous System Diseases
C0553723 BXGD009416 Squamous cell carcinoma of skin Neoplasms; Skin and Connective Tissue Diseases
C0555198 BXGD009432 Malignant Glioma Neoplasms
C0557874 BXGD009444 Global developmental delay
C0558165 BXGD009449 Curly hair (finding)
C0558356 BXGD009453 Malignant melanoma of eye Neoplasms; Eye Diseases
C0574974 BXGD009508 Finger joint hypermobility
C0575158 BXGD009515 Kyphoscoliosis deformity of spine Musculoskeletal Diseases
C0576093 BXGD009525 Knee joint valgus deformity Musculoskeletal Diseases
C0578038 BXGD009542 Thin lips
C0578682 BXGD009552 Madarosis of eyebrow Pathological Conditions, Signs and Symptoms; Eye Diseases; Skin and Connective Tissue Diseases
C0581342 BXGD009560 Redundant skin Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0585442 BXGD009593 Osteosarcoma of bone Neoplasms
C0587248 BXGD009617 Costello syndrome (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0596263 BXGD009639 Carcinogenesis Pathological Conditions, Signs and Symptoms; Neoplasms
C0598935 BXGD009674 Tumor Initiation Pathological Conditions, Signs and Symptoms; Neoplasms
C0600033 BXGD009682 Acquired Kyphoscoliosis Musculoskeletal Diseases
C0600139 BXGD009695 Prostate carcinoma Neoplasms; Male Urogenital Diseases
C0677607 BXGD009721 Hashimoto Disease Endocrine System Diseases
C0677865 BXGD009732 Brain Stem Glioma Neoplasms; Nervous System Diseases
C0677886 BXGD009734 Epithelial ovarian cancer Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0677898 BXGD009735 invasive cancer Neoplasms
C0677932 BXGD009736 Progressive Neoplastic Disease
C0677936 BXGD009737 Refractory cancer Neoplasms
C0677944 BXGD009738 Sentinel node (disorder)
C0677948 BXGD009739 Stage II Colorectal Cancer Digestive System Diseases; Neoplasms
C0677949 BXGD009740 Stage III Colorectal Cancer Digestive System Diseases; Neoplasms
C0677950 BXGD009741 Stage IV Colorectal Cancer Digestive System Diseases; Neoplasms
C0678222 BXGD009749 Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0678230 BXGD009750 Congenital Epicanthus
C0684249 BXGD009790 Carcinoma of lung Neoplasms; Respiratory Tract Diseases
C0684686 BXGD009801 Secondary malignant neoplasm of soft tissues Neoplasms
C0685938 BXGD009829 Malignant neoplasm of gastrointestinal tract Digestive System Diseases; Neoplasms
C0686377 BXGD009834 CNS metastases Neoplasms; Nervous System Diseases
C0686619 BXGD009835 Secondary malignant neoplasm of lymph node Pathological Conditions, Signs and Symptoms; Neoplasms
C0687720 BXGD009844 Central Diabetes Insipidus Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases
C0694563 BXGD009854 Excessive daytime somnolence
C0699790 BXGD009866 Colon Carcinoma Digestive System Diseases; Neoplasms
C0699791 BXGD009867 Stomach Carcinoma Digestive System Diseases; Neoplasms
C0699885 BXGD009869 Carcinoma of bladder Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0699893 BXGD009871 Skin carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0700095 BXGD009875 Central neuroblastoma Neoplasms; Nervous System Diseases
C0700199 BXGD009878 Multiple nevi Neoplasms; Skin and Connective Tissue Diseases
C0740277 BXGD009972 Bile duct carcinoma Digestive System Diseases; Neoplasms
C0740457 BXGD010000 Malignant neoplasm of kidney Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0741899 BXGD010042 Poorly differentiated carcinoma
C0742468 BXGD010063 Central nervous system lesion
C0742965 BXGD010071 Eosinophilic cystitis Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0743086 BXGD010075 Granulomatous dermatitis Skin and Connective Tissue Diseases
C0744333 BXGD010093 Gastrointestinal polyps Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0746408 BXGD010142 mass lesion
C0750935 BXGD010257 Cerebral Astrocytoma Neoplasms
C0750936 BXGD010258 Intracranial Astrocytoma Neoplasms
C0750952 BXGD010263 Biliary Tract Cancer Digestive System Diseases; Neoplasms
C0750974 BXGD010270 Brain Tumor, Primary Neoplasms; Nervous System Diseases
C0751061 BXGD010309 Craniopharyngioma, Child Neoplasms
C0751297 BXGD010384 Leptomeningeal Neoplasms Neoplasms; Nervous System Diseases
C0751396 BXGD010425 Well Differentiated Oligodendroglioma Neoplasms
C0751606 BXGD010523 Adult Acute Lymphocytic Leukemia
C0751690 BXGD010553 Malignant Peripheral Nerve Sheath Tumor Neoplasms; Nervous System Diseases
C0751691 BXGD010554 Perineurioma Neoplasms; Nervous System Diseases
C0752244 BXGD010699 Rathke Cleft Cysts Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C0796004 BXGD010776 Kabuki make-up syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Otorhinolaryngologic Diseases; Hemic and Lymphatic Diseases
C0796074 BXGD010793 MOHR-TRANEBJAERG SYNDROME Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Nervous System Diseases; Mental Disorders; Otorhinolaryngologic Diseases; Behavior and Behavior Mechanisms
C0796418 BXGD010832 Visual Pathway Glioma Neoplasms
C0812413 BXGD010847 Malignant Pleural Mesothelioma Neoplasms; Respiratory Tract Diseases
C0848558 BXGD010882 Hypospadias Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0848860 BXGD010888 endocrine carcinoma
C0849748 BXGD010890 caruncle Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0850639 BXGD010900 premalignant lesion
C0852711 BXGD010951 Sickle Cell Dactylitis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Chemically-Induced Disorders; Hemic and Lymphatic Diseases
C0854021 BXGD010990 Abnormal visual field test
C0854750 BXGD011029 Colorectal cancer recurrent Digestive System Diseases; Neoplasms
C0854917 BXGD011050 Rhabdoid Tumor of the Kidney Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0854923 BXGD011051 Mucinous endometrial carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0854985 BXGD011055 Adenocarcinoma of lung, stage I
C0855139 BXGD011076 Monocytoid B-cell lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0855740 BXGD011086 Abnormal platelet function
C0858252 BXGD011172 Breast adenocarcinoma Neoplasms; Skin and Connective Tissue Diseases
C0860594 BXGD011234 Malignant melanoma, metastatic Neoplasms
C0862506 BXGD011261 Borderline ovarian tumour
C0869083 BXGD011303 Other specified congenital malformation syndromes, not elsewhere classified in ICD10CM
C0870082 BXGD011309 Hyperkeratosis Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0878500 BXGD011365 Intraepithelial Neoplasia Neoplasms
C0878544 BXGD011368 Cardiomyopathies Cardiovascular Diseases
C0878660 BXGD011381 Proportionate short stature Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases
C0878675 BXGD011384 Erdheim-Chester Disease Hemic and Lymphatic Diseases
C0879615 BXGD011394 Stromal Neoplasm Neoplasms
C0917798 BXGD011409 Cerebral Ischemia Nervous System Diseases; Cardiovascular Diseases
C0917804 BXGD011413 Arteriovenous Malformations, Cerebral Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
C0919267 BXGD011426 ovarian neoplasm Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0919645 BXGD011433 Tumour ulceration
C0920184 BXGD011457 Fundic gland polyp Pathological Conditions, Signs and Symptoms
C0920269 BXGD011462 Microsatellite Instability Pathological Conditions, Signs and Symptoms
C0920350 BXGD011466 Autoimmune thyroiditis Immune System Diseases; Endocrine System Diseases
C0936282 BXGD011487 Blastoma Neoplasms
C0940937 BXGD011490 precancerous lesions
C0948387 BXGD011535 Secondary Adrenal Insufficiency Endocrine System Diseases
C0948775 BXGD011553 High weight Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases
C0949059 BXGD011568 Polyp of large intestine Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Neoplasms
C0949541 BXGD011578 Hurthle Cell Tumor Neoplasms
C1096063 BXGD011600 Drug Resistant Epilepsy Nervous System Diseases
C1096168 BXGD011606 Chromosome 17 trisomy Pathological Conditions, Signs and Symptoms
C1134719 BXGD011688 Invasive Ductal Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C1136033 BXGD011703 Cutaneous Mastocytosis Neoplasms; Skin and Connective Tissue Diseases
C1140680 BXGD011718 Malignant neoplasm of ovary Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C1142025 BXGD011727 Stage IV Esophageal Squamous Cell Carcinoma Digestive System Diseases; Neoplasms
C1153706 BXGD011769 Endometrial adenocarcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C1167791 BXGD011776 Skin toxicity
C1168401 BXGD011792 Squamous cell carcinoma of the head and neck Neoplasms
C1176475 BXGD011798 Ductal Carcinoma Neoplasms
C1260325 BXGD011826 Dendritic Cell Sarcoma, Follicular Neoplasms; Hemic and Lymphatic Diseases
C1260326 BXGD011827 Dendritic Cell Sarcoma, Interdigitating Neoplasms; Hemic and Lymphatic Diseases
C1261473 BXGD011855 Sarcoma Neoplasms
C1262091 BXGD011867 Lymphocytic infiltration
C1263887 BXGD011903 Neoplasm of temporal lobe Neoplasms; Nervous System Diseases
C1265996 BXGD011927 Large cell neuroendocrine carcinoma Neoplasms
C1266005 BXGD011930 Basaloid squamous cell carcinoma Neoplasms
C1266025 BXGD011935 Traditional Serrated Adenoma Neoplasms
C1266032 BXGD011937 Atypical carcinoid tumor Neoplasms
C1266045 BXGD011941 Metanephric adenoma Neoplasms
C1266050 BXGD011945 Poorly Differentiated Thyroid Carcinoma Neoplasms; Endocrine System Diseases
C1266051 BXGD011946 Papillary microcarcinoma
C1266111 BXGD011962 Glomus tumor, malignant Neoplasms
C1266112 BXGD011963 Diffuse melanocytosis Neoplasms
C1266141 BXGD011975 Nephrogenic adenofibroma Neoplasms
C1266158 BXGD011980 Nongerminomatous Germ Cell Tumor Neoplasms; Male Urogenital Diseases; Endocrine System Diseases
C1266177 BXGD011987 Dysembryoplastic neuroepithelial tumor Neoplasms
C1266184 BXGD011991 Atypical Teratoid Rhabdoid Tumor Neoplasms
C1269955 BXGD012005 Tumor Cell Invasion
C1274943 BXGD012052 Drug-induced panniculitis Skin and Connective Tissue Diseases
C1275081 BXGD012056 Cardio-facio-cutaneous syndrome Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Cardiovascular Diseases
C1275419 BXGD012083 Desmoplastic spindle and epithelioid cell melanocytic nevus of skin Neoplasms
C1292753 BXGD012226 Primary Effusion Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1298180 BXGD012246 Single tumor
C1301034 BXGD012282 Pancreatic intraepithelial neoplasia Neoplasms
C1301194 BXGD012284 Salivary duct carcinoma Neoplasms
C1302401 BXGD012303 Adenoma of large intestine Digestive System Diseases; Neoplasms
C1302808 BXGD012315 Myopericytoma Neoplasms; Skin and Connective Tissue Diseases
C1304321 BXGD012335 Eruptive melanocytic nevi
C1306214 BXGD012356 ACTH-Secreting Pituitary Adenoma Neoplasms; Nervous System Diseases; Endocrine System Diseases
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1306460 BXGD012362 Primary malignant neoplasm of lung Neoplasms; Respiratory Tract Diseases
C1306587 BXGD012368 Acute encephalopathy Nervous System Diseases
C1306759 BXGD012374 Eosinophilic disorder Hemic and Lymphatic Diseases
C1306837 BXGD012377 Papillary Renal Cell Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1314678 BXGD012387 Ameloblastic Carcinoma
C1314694 BXGD012389 Astrocytoma, low grade Neoplasms
C1318558 BXGD012403 Congenital melanocytic nevus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
C1319315 BXGD012415 Adenocarcinoma of large intestine Digestive System Diseases; Neoplasms
C1321427 BXGD012432 Epithelioid Malignant Peripheral Nerve Sheath Tumor Neoplasms; Nervous System Diseases
C1321872 BXGD012446 Stage IV Skin Melanoma Neoplasms; Skin and Connective Tissue Diseases
C1321878 BXGD012447 Desmoplastic infantile ganglioglioma
C1328931 BXGD012477 Multiple lentigines
C1332166 BXGD012493 Adenocarcinoma of the gastroesophageal junction Digestive System Diseases; Neoplasms
C1332182 BXGD012495 Adult Anaplastic Large Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332200 BXGD012501 Adult Diffuse Astrocytoma Neoplasms
C1332201 BXGD012502 Adult Diffuse Large B-Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332206 BXGD012504 Adult Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332460 BXGD012530 Barrett's Adenocarcinoma
C1332942 BXGD012558 Childhood Anaplastic Large Cell Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332965 BXGD012565 Congenital Mesoblastic Nephroma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1332969 BXGD012567 Childhood Ganglioglioma Neoplasms
C1332977 BXGD012569 Childhood Leukemia Neoplasms
C1332979 BXGD012571 Childhood Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332986 BXGD012574 Childhood Osteosarcoma Neoplasms
C1332995 BXGD012575 Childhood Pilocytic Astrocytoma Neoplasms
C1333015 BXGD012581 Childhood Kidney Wilms Tumor Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1333043 BXGD012583 Chronic Myelomonocytic Leukemia-1 Neoplasms; Hemic and Lymphatic Diseases
C1333116 BXGD012598 Colorectal Traditional Serrated Adenoma
C1333119 BXGD012600 Colorectal Villous Adenoma Neoplasms
C1333280 BXGD012609 Desmoplastic melanoma Neoplasms; Skin and Connective Tissue Diseases
C1333600 BXGD012636 Hereditary Malignant Neoplasm Neoplasms
C1333749 BXGD012638 Gallbladder Melanoma Digestive System Diseases; Neoplasms
C1333826 BXGD012649 Glomus Tumor of Uncertain Malignant Potential Neoplasms
C1333990 BXGD012670 Hereditary Nonpolyposis Colorectal Cancer Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases
C1334015 BXGD012677 High Grade Intraepithelial Neoplasia Neoplasms
C1334030 BXGD012678 Histiocytic and Dendritic Cell Neoplasm Neoplasms; Hemic and Lymphatic Diseases
C1334243 BXGD012689 Intracranial Melanoma
C1334274 BXGD012695 Invasive Carcinoma Neoplasms
C1334386 BXGD012702 Meningeal melanoma
C1334455 BXGD012711 Pulmonary Sclerosing Hemangioma Neoplasms; Respiratory Tract Diseases
C1334633 BXGD012720 Mature B-Cell Neoplasm Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1334720 BXGD012733 Metastatic Malignant Peripheral Nerve Sheath Tumor Neoplasms; Nervous System Diseases
C1334811 BXGD012742 Mucinous neoplasm
C1334953 BXGD012746 Neuroblastic tumors Neoplasms
C1335114 BXGD012763 Optic Nerve Astrocytoma Neoplasms; Eye Diseases; Nervous System Diseases
C1335177 BXGD012771 Ovarian Serous Adenocarcinoma Neoplasms
C1335302 BXGD012775 Pancreatic Ductal Adenocarcinoma Digestive System Diseases; Neoplasms; Endocrine System Diseases
C1335475 BXGD012791 Primary Carcinoma Neoplasms
C1336078 BXGD012830 Papillary renal cell carcinoma, sporadic Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1336753 BXGD012863 Thyroid Lymphoma
C1337013 BXGD012876 Differentiated Thyroid Gland Carcinoma
C1368683 BXGD012900 Epithelioma Neoplasms
C1368910 BXGD012905 Mature Teratoma Neoplasms
C1378050 BXGD012931 Oncocytic Neoplasm
C1378703 BXGD012933 Renal carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1384494 BXGD012939 Metastatic Carcinoma Pathological Conditions, Signs and Symptoms; Neoplasms
C1384666 BXGD012948 hearing impairment Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C1389016 BXGD012962 ATRIOVENTRICULAR CANAL DEFECT Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C1390474 BXGD012969 Increased susceptibility to fractures
C1402291 BXGD013015 Pigmented lesions
C1402294 BXGD013016 Primary Lesion
C1402315 BXGD013017 Vascular lesions
C1412004 BXGD013051 Tumor of the Pineal Region Neoplasms; Nervous System Diseases
C1412036 BXGD013053 Anal squamous cell carcinoma Digestive System Diseases; Neoplasms
C1455705 BXGD013103 Pulmonary Histiocytosis X Respiratory Tract Diseases; Hemic and Lymphatic Diseases
C1456781 BXGD013123 Benign melanocytic nevus Neoplasms
C1458140 BXGD013134 Bleeding tendency Hemic and Lymphatic Diseases
C1458155 BXGD013136 Mammary Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C1504404 BXGD013141 Hippocampal sclerosis
C1510472 BXGD013170 Drug Dependence Chemically-Induced Disorders; Mental Disorders
C1510502 BXGD013175 Oxyphilic Adenoma Neoplasms
C1510885 BXGD013178 Angiogenic Switch
C1511104 BXGD013179 Benign Struma Ovarii Neoplasms
C1511789 BXGD013183 Desmoplastic
C1512127 BXGD013185 HER2 gene amplification
C1512419 BXGD013189 Hereditary Melanoma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases
C1513734 BXGD013199 Solid/Multicystic Ameloblastoma Neoplasms
C1519086 BXGD013230 Pilomyxoid astrocytoma Neoplasms
C1519353 BXGD013236 Skin Papule Skin and Connective Tissue Diseases
C1519670 BXGD013241 Tumor Angiogenesis Pathological Conditions, Signs and Symptoms
C1519680 BXGD013244 Tumor Immunity Pathological Conditions, Signs and Symptoms
C1527349 BXGD013277 Ductal Breast Carcinoma Neoplasms
C1527358 BXGD013279 Phototoxicity Skin and Connective Tissue Diseases
C1527366 BXGD013280 Salaam Seizures Nervous System Diseases
C1527390 BXGD013285 Neoplasms, Intracranial Neoplasms; Nervous System Diseases
C1527404 BXGD013289 Female Pseudo-Turner Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
C1531553 BXGD013297 Dendritic cell neoplasm Neoplasms; Hemic and Lymphatic Diseases
C1535510 BXGD013319 ADENOMAS AND ADENOCARCINOMAS Neoplasms
C1535926 BXGD013322 Neurodevelopmental Disorders Mental Disorders
C1541316 BXGD013350 Adult Giant Cell Glioblastoma Neoplasms
C1541317 BXGD013351 Adult Gliosarcoma Neoplasms
C1562113 BXGD013372 Fleck corneal dystrophy Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C1565489 BXGD013401 Renal Insufficiency Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1569637 BXGD013424 Adenocarcinoma, Endometrioid Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C1608408 BXGD013434 Malignant transformation
C1611743 BXGD013456 Familial (FPAH)
C1621958 BXGD013468 Glioblastoma Multiforme Neoplasms
C1704214 BXGD013528 Lipogranuloma Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
C1704216 BXGD013529 Basaloid carcinoma Neoplasms
C1704230 BXGD013533 Grade I Astrocytoma Neoplasms
C1704231 BXGD013534 Metastatic Malignant Neoplasm to the Leptomeninges Nervous System Diseases
C1704423 BXGD013559 Milroy Disease Hemic and Lymphatic Diseases
C1707439 BXGD013583 Colorectal Mucinous Adenocarcinoma Neoplasms
C1707440 BXGD013584 Colorectal Signet Ring Cell Carcinoma Neoplasms
C1708565 BXGD013606 Invasive Cutaneous Melanoma Neoplasms; Skin and Connective Tissue Diseases
C1708604 BXGD013608 Keratocystic Odontogenic Tumor Neoplasms
C1708773 BXGD013611 Lung Melanoma Neoplasms; Respiratory Tract Diseases
C1709103 BXGD013620 Myxoinflammatory fibroblastic sarcoma
C1709457 BXGD013625 Papillary Thyroid Microcarcinoma Neoplasms; Endocrine System Diseases
C1720430 BXGD013673 Papillary carcinoma, clear cell Neoplasms
C1721098 BXGD013705 Replication Error Phenotype Pathological Conditions, Signs and Symptoms
C1827524 BXGD013773 Wide spaced nipples
C1827668 BXGD013775 Tongue thrusting when swallowing, abnormal persistence beyond early childhood Stomatognathic Diseases
C1829460 BXGD013790 Tongue thrusting Mental Disorders
C1832160 BXGD013803 Abnormality of temperature regulation
C1832348 BXGD013831 Slow-growing hair
C1832446 BXGD013844 Sparse eyebrow
C1832661 BXGD013866 ANOPHTHALMIA AND PULMONARY HYPOPLASIA Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases
C1834124 BXGD013956 Shield chest
C1835884 BXGD014061 Triangular face
C1836047 BXGD014074 Long face
C1836189 BXGD014091 Radial deviation of finger
C1836542 BXGD014129 Depressed nasal bridge
C1836543 BXGD014130 Thick vermilion border
C1836830 BXGD014165 Developmental regression Mental Disorders
C1836940 BXGD014182 Thickened nuchal skin fold
C1837142 BXGD014201 Poor suck
C1837260 BXGD014214 Prominent forehead
C1837404 BXGD014229 High, narrow palate
C1837732 BXGD014261 Thickened helices
C1837770 BXGD014270 Sparse hair
C1839364 BXGD014371 Progressive visual loss
C1839739 BXGD014400 Thick lower lip vermilion
C1839758 BXGD014402 Narrow forehead
C1839797 BXGD014409 Deep philtrum
C1840077 BXGD014434 Anteverted nostril
C1840264 BXGD014439 IMMUNE SUPPRESSION
C1842364 BXGD014511 Central hypotonia
C1843005 BXGD014548 Absent eyelashes
C1843181 BXGD014564 Noonan syndrome-like disorder with loose anagen hair Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C1843300 BXGD014572 Sparse eyelashes
C1843367 BXGD014576 Poor school performance
C1844577 BXGD014647 Hyperextensibility of the finger joints
C1845847 BXGD014760 Coarse facial features Pathological Conditions, Signs and Symptoms
C1846821 BXGD014841 Abnormality of coagulation
C1847835 BXGD014892 VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) Skin and Connective Tissue Diseases
C1847874 BXGD014894 PHACE association Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Nervous System Diseases; Cardiovascular Diseases
C1848395 BXGD014921 Large for gestational age Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
C1848760 BXGD014972 Increased anterioposterior diameter of thorax
C1849075 BXGD015002 Relative macrocephaly Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C1849172 BXGD015019 Frontal lobe hypoplasia
C1849340 BXGD015039 Long palpebral fissure
C1849367 BXGD015046 Nasal bridge wide
C1849452 BXGD015055 SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2 (disorder)
C1849667 BXGD015073 Wide nasal base
C1849677 BXGD015074 Numerous nevi Neoplasms
C1850049 BXGD015101 Clinodactyly of the 5th finger
C1851897 BXGD015245 Anterior creases of earlobe
C1853124 BXGD015304 NEPHROTIC SYNDROME, TYPE 3 Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1853141 BXGD015307 Slow decrease in visual acuity
C1853242 BXGD015322 Midface retrusion
C1854114 BXGD015383 Short nose
C1854418 BXGD015402 Biparietal narrowing
C1855728 BXGD015536 Low posterior hairline
C1857486 BXGD015710 Low-set, posteriorly rotated ears
C1857534 BXGD015715 Postnatal onset growth deficiency
C1857539 BXGD015716 Deep palmar crease
C1858091 BXGD015771 Long fingers
C1858120 BXGD015774 Generalized hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1859778 BXGD015931 Postnatal growth retardation
C1860707 BXGD015993 TUBEROUS SCLEROSIS 2 (disorder) Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C1860991 BXGD016009 NOONAN SYNDROME 3 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
C1861305 BXGD016027 TARSAL-CARPAL COALITION SYNDROME Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C1861862 BXGD016084 Familial Hypertrophic Cardiomyopathy Type 4 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C1861866 BXGD016087 Aplasia/Hypoplasia of the corpus callosum
C1861869 BXGD016088 Underdeveloped supraorbital ridges
C1861872 BXGD016089 Multiple palmar creases
C1861873 BXGD016090 Multiple plantar creases
C1861975 BXGD016095 Cafe au lait spots, multiple Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C1864795 BXGD016250 Superior pectus carinatum Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C1864796 BXGD016251 Pectus excavatum of inferior sternum
C1865014 BXGD016282 Long philtrum
C1866231 BXGD016388 Full cheeks
C1867873 BXGD016473 Failure to thrive in infancy
C1868810 BXGD016536 Neutrophilic panniculitis Skin and Connective Tissue Diseases
C1869123 BXGD016553 Limb-girdle muscular dystrophy type 2A Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases
C1956257 BXGD016623 Pulmonary Stenosis Cardiovascular Diseases
C1956346 BXGD016627 Coronary Artery Disease Cardiovascular Diseases
C1959632 BXGD016645 Plasma Cell Neoplasm Neoplasms
C1961099 BXGD016672 Precursor T-Cell Lymphoblastic Leukemia-Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1961102 BXGD016673 Precursor Cell Lymphoblastic Leukemia Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1961121 BXGD016675 Congenital vascular anomaly Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C1962966 BXGD016678 Retinopathy, CTCAE
C1963094 BXGD016681 Dry Skin, CTCAE
C1963099 BXGD016682 Myelodysplasia, CTCAE
C1963184 BXGD016688 Nystagmus, CTCAE 3.0
C1969623 BXGD016782 NEUROFIBROMATOSIS, TYPE 1-LIKE SYNDROME Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C1997217 BXGD016859 Low grade glioma Neoplasms
C2004493 BXGD016875 Leukemia, B-Cell Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C2076600 BXGD016912 Influenza due to Influenza A virus subtype H1N1 Infections; Respiratory Tract Diseases
C2237142 BXGD016960 Moderate global developmental delay
C2239176 BXGD016965 Liver carcinoma Digestive System Diseases; Neoplasms
C2242657 BXGD016989 Metastatic ocular melanoma
C2243051 BXGD017008 Large head (disorder)
C2267233 BXGD017017 Neonatal Hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C2347613 BXGD017039 Childhood Atypical Teratoid/Rhabdoid Tumor
C2347979 BXGD017051 Rosette-forming glioneuronal tumor of the fourth ventricle Neoplasms; Nervous System Diseases
C2363902 BXGD017113 Glioneuronal tumor
C2609093 BXGD017165 Pancreatic neuroendocrine tumour metastatic Digestive System Diseases; Neoplasms; Endocrine System Diseases
C2674608 BXGD017250 Feeding difficulties in infancy
C2674727 BXGD017256 ASTROCYTOMA, LOW-GRADE, SOMATIC
C2676026 BXGD017321 Optic nerve dysplasia
C2717836 BXGD017510 Steroid Sulfatase Deficiency Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C2732618 BXGD017556 Sessile Serrated Adenoma/Polyp
C2739810 BXGD017566 Lentigo maligna melanoma Neoplasms; Skin and Connective Tissue Diseases
C2919142 BXGD017867 Short Stature, CTCAE
C2931019 BXGD017938 Split hand foot deformity 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C2931201 BXGD017975 Urachal adenocarcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C2931202 BXGD017976 Urachal cancer Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C2931367 BXGD018010 Thyroid cancer, follicular Neoplasms
C2931822 BXGD018068 Nasopharyngeal carcinoma Neoplasms; Stomatognathic Diseases; Otorhinolaryngologic Diseases
C2939419 BXGD018178 Secondary Neoplasm Pathological Conditions, Signs and Symptoms; Neoplasms
C2945759 BXGD018189 aggressive cancer
C2985219 BXGD018221 Papillary tumor of the pineal region Neoplasms
C2986561 BXGD018230 Spindle Cell Oncocytoma of the Adenohypophysis Neoplasms
C2986682 BXGD018238 Locally Recurrent Malignant Neoplasm
C2987120 BXGD018242 Intramucosal Adenocarcinoma Neoplasms
C3146250 BXGD018259 Stage III Colorectal Cancer AJCC v7
C3146251 BXGD018260 Stage IV Colorectal Cancer AJCC v7
C3146252 BXGD018261 Stage II Colorectal Cancer AJCC v7
C3146254 BXGD018263 Stage III Colon Cancer AJCC v7
C3150613 BXGD018311 Long toe
C3150970 BXGD018366 NOONAN SYNDROME 7
C3150971 BXGD018367 LEOPARD SYNDROME 3
C3160718 BXGD018468 PARKINSON DISEASE, LATE-ONSET
C3160815 BXGD018478 Intraductal papillary mucinous neoplasm
C3163622 BXGD018514 Papillary Meningioma Neoplasms; Nervous System Diseases
C3164374 BXGD018527 Abnormality of pulmonary valve
C3164445 BXGD018529 Abnormality of aortic valve
C3263719 BXGD018589 Primary acquired melanosis Neoplasms; Eye Diseases
C3266123 BXGD018598 Serrated polyp Pathological Conditions, Signs and Symptoms
C3266262 BXGD018600 Multiple Chronic Conditions Pathological Conditions, Signs and Symptoms
C3267126 BXGD018615 Trichodysplasia spinulosa
C3272607 BXGD018627 Colorectal Neuroendocrine Carcinoma Digestive System Diseases; Neoplasms
C3272793 BXGD018630 Filiform Serrated Adenoma
C3272809 BXGD018633 Colorectal Serrated Adenocarcinoma
C3272841 BXGD018637 MUTYH-Associate Polyposis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C3280492 BXGD018831 TUMOR PREDISPOSITION SYNDROME
C3282896 BXGD018897 Glandular papilloma Neoplasms
C3463824 BXGD018899 MYELODYSPLASTIC SYNDROME Hemic and Lymphatic Diseases
C3472608 BXGD018921 Micropapillary carcinoma
C3472623 BXGD018924 Serrated adenocarcinoma
C3489630 BXGD018939 Somatotrophinoma, Familial Neoplasms; Nervous System Diseases; Endocrine System Diseases
C3489733 BXGD018945 Oculomotor apraxia Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms; Cardiovascular Diseases
C3495721 BXGD019001 Spitzoid melanoma
C3501843 BXGD019027 Nonmedullary Thyroid Carcinoma Neoplasms; Endocrine System Diseases
C3501844 BXGD019028 Familial Nonmedullary Thyroid Cancer Neoplasms; Endocrine System Diseases
C3501846 BXGD019029 Noonan-Like Syndrome With Loose Anagen Hair Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
C3536714 BXGD019069 Renal dysplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C3539781 BXGD019086 Progressive cGVHD
C3541994 BXGD019100 Drug Hypersensitivity Syndrome Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders
C3544205 BXGD019109 Ovarian clear cell carcinoma
C3551426 BXGD019146 Dystrophic fingernails
C3551431 BXGD019147 Sparse or absent eyelashes
C3553764 BXGD019187 Joint hyperflexibility
C3647143 BXGD019249 Secondary malignant neoplasm of ovary Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C3665349 BXGD019280 Secondary hypothyroidism Endocrine System Diseases
C3665489 BXGD019292 Borderline epithelial tumor of ovary
C3665593 BXGD019294 Melanocytic nevus of skin Neoplasms
C3697936 BXGD019363 Sialadenoma papilliferum
C3714636 BXGD019421 Pneumonitis Infections; Respiratory Tract Diseases
C3714644 BXGD019422 Thymus Neoplasms Neoplasms; Hemic and Lymphatic Diseases
C3714651 BXGD019423 Follicular Variant Thyroid Gland Papillary Carcinoma Neoplasms; Endocrine System Diseases
C3714753 BXGD019428 RETINOSCHISIS 1, X-LINKED, JUVENILE
C3714756 BXGD019429 Intellectual Disability Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C3805278 BXGD019474 Extrahepatic Cholangiocarcinoma Neoplasms
C3811653 BXGD019662 Experimental Organism Basal Cell Carcinoma Neoplasms
C3827253 BXGD019736 Classical Glioblastoma
C3839184 BXGD019770 Low grade serous carcinoma
C3839280 BXGD019772 High grade serous carcinoma
C3854181 BXGD019825 Nevus sebaceous Neoplasms
C3854222 BXGD019826 Human immunodeficiency virus (HIV) II infection category B1
C3875007 BXGD019869 Nodular thyroid disease Endocrine System Diseases
C3887461 BXGD019876 Head and Neck Carcinoma Neoplasms
C3896578 BXGD020039 Familial Colorectal Cancer Type X Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases
C3896673 BXGD020041 Familial Nonmedullary Thyroid Gland Carcinoma
C3897070 BXGD020046 Childhood Gliomatosis Cerebri Neoplasms
C3897744 BXGD020051 recurrent childhood pleomorphic xanthoastrocytoma
C3897746 BXGD020052 recurrent childhood pilocytic astrocytoma
C3898222 BXGD020065 mucosal melanoma
C3898709 BXGD020071 Intestinal-Type Sinonasal Adenocarcinoma
C3899645 BXGD020087 Childhood Pleomorphic Xanthoastrocytoma
C3899646 BXGD020088 Childhood Pilomyxoid Astrocytoma
C3899655 BXGD020091 Childhood Langerhans Cell Histiocytosis Respiratory Tract Diseases; Hemic and Lymphatic Diseases
C3899658 BXGD020092 Childhood Gliosarcoma Neoplasms
C3899659 BXGD020093 Childhood Giant Cell Glioblastoma Neoplasms
C3899662 BXGD020095 Childhood Fibrillary Astrocytoma Neoplasms
C3899668 BXGD020097 Childhood Diffuse Astrocytoma Neoplasms
C3899676 BXGD020099 Childhood Anaplastic Oligoastrocytoma
C3900100 BXGD020108 Adult Langerhans Cell Histiocytosis Respiratory Tract Diseases; Hemic and Lymphatic Diseases
C3900101 BXGD020109 Adult Germ Cell Tumor Neoplasms
C4020962 BXGD020512 Enlarged thorax
C4020968 BXGD020516 Abnormal localization of kidney
C4021095 BXGD020550 Abnormal hypothalamus morphology
C4021242 BXGD020592 Hypoplasia of the zygomatic bone
C4021250 BXGD020596 Intracranial cystic lesion Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C4021533 BXGD020656 Severe sensorineural hearing impairment Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C4021662 BXGD020726 Abnormal endocardium morphology Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C4021776 BXGD020772 Abnormality of the voice
C4021789 BXGD020781 Abnormality of the vertebral column
C4021873 BXGD020824 Abnormality of the frontal bone
C4021956 BXGD020839 Aplasia/Hypoplasia of the eyebrow
C4022755 BXGD020984 Functional abnormality of the gastrointestinal tract
C4022855 BXGD021013 Abnormal involuntary eye movements
C4023205 BXGD021143 Neoplasm of the anterior pituitary Neoplasms; Nervous System Diseases; Endocrine System Diseases
C4023385 BXGD021170 Aplasia of the semicircular canal
C4023397 BXGD021175 Abnormal hair quantity
C4023637 BXGD021234 Abnormality of the nasal bone
C4023909 BXGD021272 Aplasia/Hypoplasia of the abdominal wall musculature
C4024220 BXGD021308 Hypomelanotic macule Skin and Connective Tissue Diseases
C4024692 BXGD021371 Reduced factor XIII activity
C4024760 BXGD021408 Progressive visual field defects
C4024878 BXGD021453 Generalized hyperpigmentation Skin and Connective Tissue Diseases
C4024890 BXGD021458 Excessive wrinkled skin
C4024989 BXGD021515 Hereditary nonpolyposis colorectal carcinoma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases
C4025662 BXGD021716 Abnormality of the ulna
C4025749 BXGD021773 Abnormality of the spleen
C4025759 BXGD021780 Abnormal mitral valve morphology
C4025846 BXGD021826 Abnormality of vision
C4041089 BXGD021874 Poorly differentiated sarcoma Neoplasms
C4048329 BXGD021904 Immunosuppression
C4049272 BXGD021918 Tumour budding
C4049491 BXGD021937 Verrucous keratosis
C4053521 BXGD021967 Hemosiderotic Fibrolipomatous Tumor
C4072828 BXGD022005 Sudden loss of visual acuity
C4073145 BXGD022048 Hyperkeratosis pilaris
C4073184 BXGD022062 Thick hair
C4085873 BXGD022121 LUSCAN-LUMISH SYNDROME
C4086152 BXGD022123 Childhood Astrocytoma Neoplasms
C4086165 BXGD022126 Childhood Neuroblastoma Neoplasms
C4086178 BXGD022128 Childhood Thyroid Gland Papillary Carcinoma Neoplasms; Endocrine System Diseases
C4087124 BXGD022132 Immunoglobulin G4-Related Disease Immune System Diseases
C4087141 BXGD022133 Skin squamous cell carcinoma metastatic
C4225426 BXGD022276 THYROID CANCER, NONMEDULLARY, 2
C4281993 BXGD022418 Neonatal respiratory distress Respiratory Tract Diseases
C4282128 BXGD022420 PATENT DUCTUS ARTERIOSUS 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C4282407 BXGD022423 Sparse and thin eyebrow
C4283858 BXGD022426 Anaplastic Pleomorphic Xanthoastrocytoma Neoplasms
C4283978 BXGD022427 Primary adenocarcinoma of lower third of esophagus due to Barrett esophagus
C4284013 BXGD022428 Primary cholangiocarcinoma of intrahepatic biliary tract Neoplasms
C4287590 BXGD022470 Thyroid Gland Noninvasive Follicular Neoplasm with Papillary-Like Nuclear Features Neoplasms; Endocrine System Diseases
C4289580 BXGD022491 Epithelioid glioblastoma
C4289690 BXGD022494 Diffuse Glioma Neoplasms
C4296896 BXGD022519 Hyperplastic polyposis syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C4317109 BXGD022725 Epileptic Seizures Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C4477013 BXGD022904 Impaired oropharyngeal swallow response Digestive System Diseases; Otorhinolaryngologic Diseases
C4509816 BXGD022975 Squamous non-small cell lung cancer Neoplasms; Respiratory Tract Diseases
C4511687 BXGD023010 Pancreatic Intraductal Papillary Mucinous Neoplasm Digestive System Diseases; Neoplasms; Endocrine System Diseases
C4520731 BXGD023036 Stage II Cutaneous Melanoma AJCC v6 and v7
C4520732 BXGD023037 Stage IV Cutaneous Melanoma AJCC v6 and v7
C4520764 BXGD023038 Stage 0 Cutaneous Melanoma AJCC v6 and v7
C4522181 BXGD023074 Brachial Amyotrophic Diplegia Nervous System Diseases
C4523846 BXGD023079 MSI-high
C4524211 BXGD023101 Sellar lesion
C4524257 BXGD023102 MSI-low
C4524268 BXGD023104 Advanced lung cancer
C4525124 BXGD023120 Stage III Colon Cancer AJCC v8
C4525297 BXGD023131 Stage 0 Gallbladder Cancer AJCC v8
C4525300 BXGD023132 Stage IIA Gallbladder Cancer AJCC v8
C4525301 BXGD023133 Stage IIB Gallbladder Cancer AJCC v8
C4525302 BXGD023134 Stage III Gallbladder Cancer AJCC v8
C4525305 BXGD023135 Stage IV Gallbladder Cancer AJCC v8
C4526729 BXGD023150 Refractory Erdheim-Chester Disease Hemic and Lymphatic Diseases
C4544822 BXGD023286 Microsatellite instability-high colorectal cancer Digestive System Diseases; Neoplasms
C4551472 BXGD023303 Hypertrophic obstructive cardiomyopathy Cardiovascular Diseases
C4551484 BXGD023311 Leopard Syndrome 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
C4551485 BXGD023312 Clinodactyly
C4551517 BXGD023334 Flared nostrils abnormality
C4551546 BXGD023341 Refractory Hairy Cell Leukemia Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C4551548 BXGD023342 Grade III Childhood Astrocytoma Neoplasms
C4551583 BXGD023361 Cerebral cortical atrophy
C4551602 BXGD023369 Noonan Syndrome 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Cardiovascular Diseases
C4551675 BXGD023384 Keratoderma, Palmoplantar Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C4551683 BXGD023389 Adrenal Gland Pheochromocytoma Neoplasms; Endocrine System Diseases
C4551686 BXGD023391 Malignant neoplasm of soft tissue Neoplasms
C4552097 BXGD023487 Nevus Sebaceus of Jadassohn Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C4552100 BXGD023488 Lynch Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms; Nutritional and Metabolic Diseases
C4553962 BXGD023553 Hyperkeratosis, CTCAE
C4554036 BXGD023557 Nystagmus, CTCAE 5.0
C4684942 BXGD023578 Refractory Thyroid Gland Carcinoma Neoplasms; Endocrine System Diseases
C4688319 BXGD023586 Refractory Melanoma Neoplasms
C4721411 BXGD023735 Osteolysis Musculoskeletal Diseases
C4721414 BXGD023738 Mantle cell lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C4721532 BXGD023752 Lymphoma, Non-Hodgkin, Familial Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C4721579 BXGD023759 Secondary malignant neoplasm of colon and/or rectum Digestive System Diseases; Neoplasms
C4721610 BXGD023760 Carcinoma, Ovarian Epithelial Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C4721806 BXGD023772 Carcinoma, Basal Cell Neoplasms
C4722085 BXGD023788 Malignant neoplasm of colon and/or rectum
C4722099 BXGD023789 High grade glioma Neoplasms
C4722172 BXGD023791 Primary differentiated carcinoma of thyroid gland
C4725091 BXGD023828 metastatic intraocular melanoma Neoplasms; Eye Diseases
C4725093 BXGD023830 Unresectable Melanoma Neoplasms
C4725861 BXGD023840 Metastatic Malignant Neoplasm in the Viscera
C4727838 BXGD023874 Advanced Melanoma
C4733213 BXGD023913 stage IIIB melanoma
C4733333 BXGD023920 familial non-medullary thyroid cancer Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C4733534 BXGD023923 stage IVC anaplastic thyroid cancer
C4733538 BXGD023925 recurrent papillary thyroid cancer Neoplasms; Endocrine System Diseases
C4744444 BXGD023941 Metastatic Lung Adenocarcinoma Neoplasms
C4744527 BXGD023944 Temporal Lobe Pleomorphic Xanthoastrocytoma
C4744564 BXGD023947 Metastatic Colorectal Carcinoma Digestive System Diseases; Neoplasms
C4749367 BXGD024057 Mesial temporal lobe epilepsy with hippocampal sclerosis Nervous System Diseases
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0000434 Ethanol 46.07
BXGC0000436 Glycerol 92.09
BXGC0000441 Dimethyl sulfoxide 78.13
BXGC0002063 Alternariol 258.23
BXGC0002588 Magnesium 24.31
BXGC0003705 Chloride 35.45
BXGC0004580 Carbanilide 212.25
BXGC0004705 Diphenylamine 169.22
BXGC0005625 alpha-D-Glucopyranose 180.16
BXGC0005683 Quercetin 302.24
BXGC0006193 Ellagic acid 302.19
BXGC0006306 Myricetin 318.24
BXGC0016254 Dehydroabietic Acid 300.21
BXGC0017701 Altenusin 290.08
BXGC0023872 Adenine 135.05
BXGC0035685 alternariol monomethyl ether 272.07
BXGC0042376 Picropodophyllotoxin 414.13
BXGC0045254 Sb-202190 331.11
BXGC0047692 Gefitinib 446.15
BXGC0050099 (2E,5S,6S,8Z,11S)-5,6,15-Trihydroxy-17-Methoxy-11-Methyl-12-Oxabicyclo[12.4.0]Octadeca-1(14),2,8,15,17-Pentaene-7,13-Dione 362.14
BXGC0051819 Altertoxin I 352.09
The  target protein-related  foods
Foods
BXGF Id Food Name Scientific Name Food Group Number of compound? Number of compound in food, higher numbers indicate the food are more associated with the protein