Showing entry for Proto-oncogene tyrosine-protein kinase receptor Ret


　 　 　 　 　 　 　 　 　 　 　 　
General Target Information
BXGT IdBXGT006703
Protein NameProto-oncogene tyrosine-protein kinase receptor Ret
Uniport IdP07949
GeneRET
Gene Id5979
DomainCadherin; Pkinase_Tyr; RET_CLD1; RET_CLD3; RET_CLD4
Pfam PF00028   PF07714   PF17756   PF17812   PF17813  
OrganismHomo sapiens (Human)
Target protein  affiliated  biological  pathways
KEGG
Class Subclass KEGG Id Pathway Name
6. Human Diseases 6.1 Cancers: Overview hsa05200 Pathways in cancer
6. Human Diseases 6.2 Cancers: Specific types hsa05216 Thyroid cancer
6. Human Diseases 6.1 Cancers: Overview hsa05230 Central carbon metabolism in cancer
Gene Ontology
GO Type GO Id Gene Ontology
Biological Process GO:0006919 activation of cysteine-type endopeptidase activity involved in apoptotic process
Biological Process GO:0000187 activation of MAPK activity
Biological Process GO:0007411 axon guidance
Biological Process GO:0071300 cellular response to retinoic acid
Biological Process GO:0001838 embryonic epithelial tube formation
Biological Process GO:0048484 enteric nervous system development
Biological Process GO:0035860 glial cell-derived neurotrophic factor receptor signaling pathway
Biological Process GO:0007156 homophilic cell adhesion via plasma membrane adhesion molecules
Biological Process GO:0060384 innervation
Biological Process GO:0097021 lymphocyte migration into lymphoid organs
Biological Process GO:0000165 MAPK cascade
Biological Process GO:0033619 membrane protein proteolysis
Biological Process GO:0007275 multicellular organism development
Biological Process GO:0001755 neural crest cell migration
Biological Process GO:0007158 neuron cell-cell adhesion
Biological Process GO:0042551 neuron maturation
Biological Process GO:0061146 Peyer's patch morphogenesis
Biological Process GO:0033630 positive regulation of cell adhesion mediated by integrin
Biological Process GO:0030335 positive regulation of cell migration
Biological Process GO:0045793 positive regulation of cell size
Biological Process GO:2001241 positive regulation of extrinsic apoptotic signaling pathway in absence of ligand
Biological Process GO:0033674 positive regulation of kinase activity
Biological Process GO:0043410 positive regulation of MAPK cascade
Biological Process GO:0072300 positive regulation of metanephric glomerulus development
Biological Process GO:0014042 positive regulation of neuron maturation
Biological Process GO:0010976 positive regulation of neuron projection development
Biological Process GO:0033141 positive regulation of peptidyl-serine phosphorylation of STAT protein
Biological Process GO:0051897 positive regulation of protein kinase B signaling
Biological Process GO:0045893 positive regulation of transcription, DNA-templated
Biological Process GO:0007497 posterior midgut development
Biological Process GO:0006468 protein phosphorylation
Biological Process GO:0050770 regulation of axonogenesis
Biological Process GO:0030155 regulation of cell adhesion
Biological Process GO:0042493 response to drug
Biological Process GO:0048265 response to pain
Biological Process GO:0060041 retina development in camera-type eye
Biological Process GO:0007165 signal transduction
Biological Process GO:0007169 transmembrane receptor protein tyrosine kinase signaling pathway
Biological Process GO:0001657 ureteric bud development
Biological Process GO:0035799 ureter maturation
molecular function GO:0005524 ATP binding
molecular function GO:0005509 calcium ion binding
molecular function GO:0004713 protein tyrosine kinase activity
molecular function GO:0038023 signaling receptor activity
molecular function GO:0004714 transmembrane receptor protein tyrosine kinase activity
cellular component GO:0030424 axon
cellular component GO:0030425 dendrite
cellular component GO:0005769 early endosome
cellular component GO:0010008 endosome membrane
cellular component GO:0005887 integral component of plasma membrane
cellular component GO:0045121 membrane raft
cellular component GO:0043025 neuronal cell body
cellular component GO:0005886 plasma membrane
cellular component GO:0098797 plasma membrane protein complex
cellular component GO:0043235 receptor complex
Reactome
Pathway Id Pathway Name
R-HSA-1266738 Developmental Biology
R-HSA-1280215 Cytokine Signaling in Immune system
R-HSA-162582 Signal Transduction
R-HSA-168256 Immune System
R-HSA-422475 Axon guidance
R-HSA-5673001 RAF/MAP kinase cascade
R-HSA-5683057 MAPK family signaling cascades
R-HSA-5684996 MAPK1/MAPK3 signaling
R-HSA-8853659 RET signaling
R-HSA-9607240 FLT3 Signaling
R-HSA-9675108 Nervous system development
Target protein-related  diseases
Disease
CUI Id BXGD Id Disease Name Disease Class
C0000731 BXGD000002 Abdomen distended Digestive System Diseases
C0000737 BXGD000005 Abdominal Pain Pathological Conditions, Signs and Symptoms
C0000768 BXGD000007 Congenital Abnormality Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0000846 BXGD000015 Agenesis
C0001193 BXGD000030 Apert syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0001206 BXGD000033 Acromegaly Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases
C0001418 BXGD000050 Adenocarcinoma Neoplasms
C0001430 BXGD000054 Adenoma Neoplasms
C0001618 BXGD000063 Tumors of Adrenal Cortex Neoplasms; Endocrine System Diseases
C0001624 BXGD000067 Adrenal Gland Neoplasms Neoplasms; Endocrine System Diseases
C0001815 BXGD000078 Primary Myelofibrosis Hemic and Lymphatic Diseases
C0001973 BXGD000095 Alcoholic Intoxication, Chronic Chemically-Induced Disorders; Mental Disorders
C0002395 BXGD000111 Alzheimer's Disease Nervous System Diseases; Mental Disorders
C0002726 BXGD000125 Amyloidosis Nutritional and Metabolic Diseases
C0002736 BXGD000127 Amyotrophic Lateral Sclerosis Nutritional and Metabolic Diseases; Nervous System Diseases
C0002793 BXGD000130 Anaplasia Pathological Conditions, Signs and Symptoms; Neoplasms
C0002893 BXGD000150 Refractory anemias Hemic and Lymphatic Diseases
C0003076 BXGD000171 Aniridia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0003578 BXGD000211 Apnea Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C0003873 BXGD000236 Rheumatoid Arthritis Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases
C0004135 BXGD000257 Ataxia Telangiectasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases; Nervous System Diseases; Cardiovascular Diseases
C0004779 BXGD000291 Basal Cell Nevus Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Musculoskeletal Diseases; Stomatognathic Diseases
C0005874 BXGD000344 Blushing Behavior and Behavior Mechanisms
C0006118 BXGD000372 Brain Neoplasms Neoplasms; Nervous System Diseases
C0006142 BXGD000374 Malignant neoplasm of breast Neoplasms; Skin and Connective Tissue Diseases
C0006413 BXGD000397 Burkitt Lymphoma Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases
C0006826 BXGD000408 Malignant Neoplasms Neoplasms
C0007095 BXGD000423 Carcinoid Tumor Neoplasms
C0007097 BXGD000424 Carcinoma Neoplasms
C0007102 BXGD000425 Malignant tumor of colon Digestive System Diseases; Neoplasms
C0007115 BXGD000432 Malignant neoplasm of thyroid Neoplasms; Endocrine System Diseases
C0007124 BXGD000437 Noninfiltrating Intraductal Carcinoma 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
C0007786 BXGD000486 Brain Ischemia Nervous System Diseases; Cardiovascular Diseases
C0007787 BXGD000487 Transient Ischemic Attack Nervous System Diseases; Cardiovascular Diseases
C0008031 BXGD000511 Chest Pain Pathological Conditions, Signs and Symptoms
C0008073 BXGD000518 Developmental Disabilities Mental Disorders
C0008525 BXGD000554 Choroideremia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C0008626 BXGD000559 Congenital chromosomal disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C0008925 BXGD000575 Cleft Palate Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases
C0009081 BXGD000581 Congenital clubfoot Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0009319 BXGD000596 Colitis Digestive System Diseases
C0009402 BXGD000605 Colorectal Carcinoma Digestive System Diseases; Neoplasms
C0009404 BXGD000606 Colorectal Neoplasms Digestive System Diseases; Neoplasms
C0009806 BXGD000633 Constipation Pathological Conditions, Signs and Symptoms
C0010481 BXGD000673 Cushing Syndrome Endocrine System Diseases
C0010709 BXGD000689 Cyst Pathological Conditions, Signs and Symptoms; Neoplasms
C0011053 BXGD000694 Deafness Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0011991 BXGD000766 Diarrhea Pathological Conditions, Signs and Symptoms
C0012811 BXGD000790 Colon diverticulum anatomic structure Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0012813 BXGD000791 Diverticulitis Digestive System Diseases
C0013080 BXGD000797 Down Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0013264 BXGD000808 Muscular Dystrophy, Duchenne Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System 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
C0013363 BXGD000818 Dysautonomia Nervous System Diseases
C0014130 BXGD000899 Endocrine System Diseases Endocrine System Diseases
C0014132 BXGD000900 Endocrine Gland Neoplasms Neoplasms; Endocrine System Diseases
C0014356 BXGD000910 Enterocolitis Digestive System Diseases
C0014518 BXGD000921 Toxic Epidermal Necrolysis Skin and Connective Tissue Diseases; Immune System Diseases; Chemically-Induced Disorders; Stomatognathic Diseases
C0014544 BXGD000926 Epilepsy Nervous System Diseases
C0014848 BXGD000955 Esophageal Achalasia Digestive System Diseases
C0015544 BXGD001003 Failure to Thrive Pathological Conditions, Signs and Symptoms
C0015672 BXGD001011 Fatigue Pathological Conditions, Signs and Symptoms
C0016045 BXGD001037 fibroma Neoplasms
C0016057 BXGD001042 Fibrosarcoma Neoplasms
C0016382 BXGD001054 Flushing Pathological Conditions, Signs and Symptoms
C0016842 BXGD001083 Congenital pectus excavatum Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0017075 BXGD001089 Ganglioneuroma Neoplasms
C0017168 BXGD001101 Gastroesophageal reflux disease Digestive System Diseases
C0017178 BXGD001102 Gastrointestinal Diseases Digestive System Diseases
C0017636 BXGD001131 Glioblastoma Neoplasms
C0017653 BXGD001135 Glomus Tumor Neoplasms
C0017658 BXGD001138 Glomerulonephritis Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0018021 BXGD001162 Goiter Endocrine System Diseases
C0018023 BXGD001164 Nodular Goiter Endocrine System Diseases
C0018213 BXGD001187 Graves Disease Eye Diseases; Immune System Diseases; Endocrine System Diseases
C0018552 BXGD001202 Hamartoma Neoplasms
C0018553 BXGD001203 Hamartoma Syndrome, Multiple Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C0018777 BXGD001217 Conductive hearing loss Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0018784 BXGD001220 Sensorineural Hearing Loss (disorder) Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0018802 BXGD001227 Congestive heart failure Cardiovascular Diseases
C0018916 BXGD001245 Hemangioma Neoplasms
C0018923 BXGD001248 Hemangiosarcoma Neoplasms
C0018965 BXGD001258 Hematuria Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0019562 BXGD001336 Von Hippel-Lindau Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
C0019569 BXGD001337 Hirschsprung Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
C0019618 BXGD001339 Histiocytosis Hemic and Lymphatic Diseases
C0019829 BXGD001350 Hodgkin Disease Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0020074 BXGD001358 HSAN Type IV Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C0020179 BXGD001363 Huntington Disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders
C0020224 BXGD001366 Polyhydramnios Female Urogenital Diseases and Pregnancy Complications
C0020437 BXGD001381 Hypercalcemia Nutritional and Metabolic Diseases
C0020440 BXGD001383 Hypercapnia Pathological Conditions, Signs and Symptoms
C0020458 BXGD001393 Hyperhidrosis disorder Skin and Connective Tissue Diseases
C0020502 BXGD001410 Hyperparathyroidism Endocrine System Diseases
C0020503 BXGD001411 Hyperparathyroidism, Secondary Endocrine System Diseases
C0020507 BXGD001413 Hyperplasia Pathological Conditions, Signs and Symptoms
C0020534 BXGD001421 Orbital separation excessive Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0020598 BXGD001440 Hypocalcemia Nutritional and Metabolic Diseases
C0020676 BXGD001462 Hypothyroidism Endocrine System Diseases
C0021368 BXGD001502 Inflammation Pathological Conditions, Signs and Symptoms
C0021843 BXGD001520 Intestinal Obstruction Digestive System Diseases
C0021847 BXGD001523 Intestinal Pseudo-Obstruction Digestive System Diseases
C0022104 BXGD001529 Irritable Bowel Syndrome Digestive System Diseases
C0022661 BXGD001572 Kidney Failure, Chronic Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022681 BXGD001577 Medullary sponge kidney Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0022821 BXGD001590 Kyphosis deformity of spine Musculoskeletal Diseases
C0023418 BXGD001642 leukemia Neoplasms
C0023434 BXGD001643 Chronic Lymphocytic 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
C0023479 BXGD001663 Acute myelomonocytic leukemia Neoplasms
C0023480 BXGD001664 Leukemia, Myelomonocytic, Chronic Neoplasms; Hemic and Lymphatic Diseases
C0023487 BXGD001669 Acute Promyelocytic Leukemia Neoplasms
C0023827 BXGD001707 liposarcoma Neoplasms
C0024003 BXGD001726 Lordosis Musculoskeletal Diseases
C0024115 BXGD001732 Lung diseases Respiratory Tract Diseases
C0024121 BXGD001735 Lung Neoplasms Neoplasms; Respiratory Tract Diseases
C0024141 BXGD001740 Lupus Erythematosus, Systemic Skin and Connective Tissue Diseases; Immune System Diseases
C0024299 BXGD001758 Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C0024623 BXGD001791 Malignant neoplasm of stomach Digestive System Diseases; Neoplasms
C0025149 BXGD001826 Medulloblastoma Neoplasms
C0025160 BXGD001827 Megacolon Digestive System Diseases
C0025202 BXGD001832 melanoma Neoplasms
C0025209 BXGD001834 Melanosis Skin and Connective Tissue Diseases
C0025237 BXGD001841 Melnick-Needles Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0025267 BXGD001845 Multiple Endocrine Neoplasia Type 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
C0025268 BXGD001846 Multiple Endocrine Neoplasia Type 2a Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
C0025269 BXGD001847 Multiple Endocrine Neoplasia Type 2b Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
C0026633 BXGD001910 Mouth Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C0026764 BXGD001928 Multiple Myeloma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases; Cardiovascular Diseases
C0026827 BXGD001936 Muscle hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0026848 BXGD001941 Myopathy Musculoskeletal Diseases; Nervous System Diseases
C0027022 BXGD001962 Myeloproliferative disease Hemic and Lymphatic Diseases
C0027497 BXGD001993 Nausea Pathological Conditions, Signs and Symptoms
C0027498 BXGD001994 Nausea and vomiting Pathological Conditions, Signs and Symptoms
C0027627 BXGD002006 Neoplasm Metastasis Pathological Conditions, Signs and Symptoms; Neoplasms
C0027651 BXGD002009 Neoplasms Neoplasms
C0027662 BXGD002015 Multiple Endocrine Neoplasia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
C0027666 BXGD002018 Neoplasms, Radiation-Induced Neoplasms; Wounds and Injuries
C0027672 BXGD002020 Neoplastic Syndromes, Hereditary Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C0027708 BXGD002025 Nephroblastoma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0027765 BXGD002033 nervous system disorder Nervous System Diseases
C0027796 BXGD002037 Neuralgia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0027809 BXGD002040 Neurilemmoma Neoplasms
C0027819 BXGD002043 Neuroblastoma Neoplasms
C0027831 BXGD002047 Neurofibromatosis 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C0028259 BXGD002073 Nodule
C0029463 BXGD002160 Osteosarcoma Neoplasms
C0030193 BXGD002191 Pain Pathological Conditions, Signs and Symptoms
C0030232 BXGD002197 Pallor Pathological Conditions, Signs and Symptoms
C0030252 BXGD002199 Palpitations Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
C0030297 BXGD002204 Pancreatic Neoplasm Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0030421 BXGD002218 Paraganglioma Neoplasms
C0030422 BXGD002219 Extra-Adrenal Paraganglioma Neoplasms
C0030472 BXGD002227 Paraneoplastic Syndromes Neoplasms
C0030517 BXGD002234 Parathyroid Diseases Endocrine System Diseases
C0030521 BXGD002235 Parathyroid Neoplasms Neoplasms; Endocrine System Diseases
C0030567 BXGD002240 Parkinson Disease Nervous System Diseases
C0031485 BXGD002303 Phenylketonurias Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
C0031511 BXGD002304 Pheochromocytoma Neoplasms
C0032002 BXGD002320 Pituitary Diseases Nervous System Diseases; Endocrine System Diseases
C0032580 BXGD002362 Adenomatous Polyposis Coli Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases; Neoplasms
C0032927 BXGD002381 Precancerous Conditions Neoplasms
C0033036 BXGD002389 Atrial Premature Complexes Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0033578 BXGD002408 Prostatic Neoplasms Neoplasms; Male Urogenital Diseases
C0033687 BXGD002415 Proteinuria Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0035067 BXGD002504 Renal Artery Stenosis Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases
C0035309 BXGD002530 Retinal Diseases Eye Diseases
C0035335 BXGD002540 Retinoblastoma Neoplasms; Eye Diseases
C0036439 BXGD002615 Scoliosis, unspecified Musculoskeletal Diseases
C0036572 BXGD002625 Seizures Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0036631 BXGD002626 Seminoma Neoplasms
C0037205 BXGD002672 Sirenomelia Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0037286 BXGD002681 Skin Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C0038220 BXGD002740 Status Epilepticus Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0038379 BXGD002752 Strabismus Eye Diseases; Nervous System Diseases
C0039231 BXGD002799 Tachycardia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0039239 BXGD002803 Sinus Tachycardia Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases
C0039273 BXGD002806 Talipes cavus Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
C0039685 BXGD002825 Tetralogy of Fallot Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular 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
C0040156 BXGD002849 Thyrotoxicosis Endocrine System Diseases
C0040250 BXGD002853 Tinea Capitis Infections; Skin and Connective Tissue Diseases
C0040588 BXGD002879 Tracheoesophageal Fistula Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Respiratory Tract Diseases
C0040822 BXGD002885 Tremor Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0041207 BXGD002898 Truncus Arteriosus, Persistent Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0041948 BXGD002939 Uremia Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0042063 BXGD002953 Urogenital Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0042580 BXGD002992 Vesico-Ureteral Reflux Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0042781 BXGD003000 Visceral Myopathy Digestive System Diseases
C0042928 BXGD003014 Vocal Cord Paralysis Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
C0042963 BXGD003018 Vomiting Pathological Conditions, Signs and Symptoms
C0079218 BXGD003066 Fibromatosis, Aggressive Neoplasms
C0079924 BXGD003103 Oligohydramnios Female Urogenital Diseases and Pregnancy Complications
C0080024 BXGD003104 Piebaldism Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
C0080032 BXGD003105 Pleural Effusion, Malignant Neoplasms; Respiratory Tract Diseases
C0085110 BXGD003126 Severe Combined Immunodeficiency Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Immune System Diseases
C0085215 BXGD003141 Ovarian Failure, Premature Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0085758 BXGD003250 Aganglionosis, Colonic Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
C0086437 BXGD003282 Joint laxity Musculoskeletal Diseases
C0086692 BXGD003306 Benign Neoplasm Neoplasms
C0086769 BXGD003310 Panic Attacks Mental Disorders
C0149782 BXGD003365 Squamous cell carcinoma of lung Neoplasms; Respiratory Tract Diseases
C0149887 BXGD003380 Slipped Capital Femoral Epiphyses Musculoskeletal Diseases
C0149925 BXGD003387 Small cell carcinoma of lung Neoplasms; Respiratory Tract Diseases
C0151468 BXGD003424 Thyroid Gland Follicular Adenoma Neoplasms; Endocrine System Diseases
C0151514 BXGD003429 Atrophic condition of skin Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0151779 BXGD003473 Cutaneous Melanoma Neoplasms; Skin and Connective Tissue Diseases
C0152013 BXGD003516 Adenocarcinoma of lung (disorder) Neoplasms
C0152132 BXGD003547 Hypertensive Retinopathy Eye Diseases; Cardiovascular Diseases
C0153425 BXGD003641 Malignant tumor of small intestine Digestive System Diseases; Neoplasms
C0153633 BXGD003674 Malignant neoplasm of brain Neoplasms; Nervous System Diseases
C0153653 BXGD003675 Malignant tumor of parathyroid gland Neoplasms; Endocrine System Diseases
C0153658 BXGD003676 Malignant neoplasm of endocrine gland Neoplasms; Endocrine System Diseases
C0153676 BXGD003679 Secondary malignant neoplasm of lung Neoplasms; Respiratory Tract Diseases
C0162316 BXGD003936 Iron deficiency anemia Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
C0162678 BXGD003974 Neurofibromatoses Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Nervous System Diseases
C0178664 BXGD004032 Glomerulosclerosis (disorder) Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Cardiovascular Diseases
C0178874 BXGD004037 Tumor Progression Pathological Conditions, Signs and Symptoms
C0205642 BXGD004094 Adenocarcinoma, Oxyphilic Neoplasms
C0205645 BXGD004097 Adenocarcinoma, Tubular Neoplasms
C0205647 BXGD004099 Follicular adenoma Neoplasms
C0205651 BXGD004103 Adenoma, Trabecular Neoplasms
C0205696 BXGD004107 Anaplastic carcinoma Neoplasms
C0205698 BXGD004109 Undifferentiated carcinoma Neoplasms
C0205851 BXGD004132 Germ cell tumor Neoplasms
C0206657 BXGD004220 Alveolar Soft Part Sarcoma Neoplasms
C0206682 BXGD004237 Follicular thyroid carcinoma Neoplasms
C0206685 BXGD004240 Acinar Cell Carcinoma Neoplasms
C0206693 BXGD004244 Medullary carcinoma Neoplasms
C0206695 BXGD004246 Carcinoma, Neuroendocrine Neoplasms
C0206718 BXGD004264 Ganglioneuroblastoma Neoplasms
C0206754 BXGD004289 Neuroendocrine Tumors Neoplasms
C0220633 BXGD004303 Uveal melanoma Neoplasms; Eye Diseases
C0220650 BXGD004310 Metastatic malignant neoplasm to brain Pathological Conditions, Signs and Symptoms; Neoplasms; Nervous System Diseases
C0221002 BXGD004360 Hyperparathyroidism, Primary Endocrine System Diseases
C0221154 BXGD004393 Paroxysmal hypertension Cardiovascular Diseases
C0221263 BXGD004427 Cafe-au-Lait Spots Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases
C0221391 BXGD004456 Melanosis coli Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Skin and Connective Tissue Diseases
C0232466 BXGD004543 Feeding difficulties
C0234119 BXGD004622 Neuromuscular inhibition
C0234958 BXGD004702 Muscle degeneration Musculoskeletal Diseases
C0235659 BXGD004763 Reduced fetal movement Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications
C0235831 BXGD004773 Renal Cell Dysplasia Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0235974 BXGD004796 Pancreatic carcinoma Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0235991 BXGD004802 Small for gestational age (disorder) Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications
C0238062 BXGD004868 Chronic intestinal pseudo-obstruction Digestive System Diseases
C0238196 BXGD004891 Small intestine carcinoma Digestive System Diseases; Neoplasms
C0238198 BXGD004893 Gastrointestinal Stromal Tumors Digestive System Diseases; Neoplasms
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
C0238790 BXGD004956 bone destruction
C0239234 BXGD004974 Low set ears
C0240066 BXGD005016 Iron deficiency Nutritional and Metabolic Diseases
C0240635 BXGD005047 Byzanthine arch palate Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases
C0242225 BXGD005143 Color blindness Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
C0242363 BXGD005156 Islet Cell Tumor Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0242379 BXGD005157 Malignant neoplasm of lung Neoplasms; Respiratory Tract Diseases
C0242422 BXGD005163 Parkinsonian Disorders Nervous System Diseases
C0243026 BXGD005210 Sepsis Pathological Conditions, Signs and Symptoms; Infections
C0243050 BXGD005212 Cardiovascular Abnormalities Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C0260037 BXGD005227 Multiple tumors Neoplasms
C0262584 BXGD005256 Carcinoma, Small Cell Neoplasms
C0262587 BXGD005259 Parathyroid Adenoma Neoplasms; Endocrine System Diseases
C0265783 BXGD005575 Congenital hypoplasia of lung Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases
C0266292 BXGD005643 Congenital anomaly of the kidney Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0266294 BXGD005644 Unilateral agenesis of kidney Pathological Conditions, Signs and Symptoms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0267373 BXGD005741 Intestinal hemorrhage NOS Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0268164 BXGD005844 Primary hyperoxaluria, type I Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0268390 BXGD005929 Muckle-Wells Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0268397 BXGD005932 Amyloidosis, Primary Cutaneous Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic 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
C0270823 BXGD006112 Petit mal status Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0271633 BXGD006223 Disorder of endocrine pancreas Pathological Conditions, Signs and Symptoms; Digestive System Diseases; Endocrine System Diseases
C0271844 BXGD006269 Parathyroid hyperplasia Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Endocrine System Diseases
C0271846 BXGD006270 Familial hyperparathyroidism Endocrine System Diseases
C0278479 BXGD006509 Stage II Colon Cancer Digestive System Diseases; Neoplasms
C0278488 BXGD006515 Carcinoma breast stage IV
C0278592 BXGD006544 Adult Angiosarcoma Neoplasms
C0278595 BXGD006545 Adult Fibrosarcoma Neoplasms
C0278608 BXGD006549 Adult Liposarcoma Neoplasms
C0278681 BXGD006558 metastatic parathyroid cancer Neoplasms; Endocrine System Diseases
C0278878 BXGD006609 Adult Glioblastoma Neoplasms
C0278883 BXGD006614 Metastatic melanoma Neoplasms
C0278987 BXGD006620 Metastatic non-small cell lung cancer Neoplasms
C0279014 BXGD006623 Childhood Germ Cell Tumor Neoplasms
C0279557 BXGD006636 Adenosquamous cell lung cancer Neoplasms; Respiratory Tract Diseases
C0279563 BXGD006637 Lobular carcinoma in situ of breast Neoplasms; Skin and Connective Tissue Diseases
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
C0279984 BXGD006703 Childhood Liposarcoma Neoplasms
C0279988 BXGD006707 Childhood Angiosarcoma Neoplasms
C0280100 BXGD006713 Solid Neoplasm Neoplasms
C0280217 BXGD006720 stage, non-small cell lung cancer Neoplasms; Respiratory Tract Diseases
C0280449 BXGD006746 secondary acute myeloid leukemia Neoplasms
C0280474 BXGD006748 Childhood Glioblastoma Neoplasms
C0280787 BXGD006761 Adult Anaplastic Ependymoma Neoplasms
C0280788 BXGD006762 Anaplastic Ependymoma Neoplasms
C0280962 BXGD006768 Bone Marrow Suppression Hemic and Lymphatic Diseases
C0281361 BXGD006774 Adenocarcinoma of pancreas Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0282313 BXGD006803 Condition, Preneoplastic Neoplasms
C0302511 BXGD006849 Small for gestational age fetus Pathological Conditions, Signs and Symptoms
C0311335 BXGD006877 Grand Mal Status Epilepticus Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0311361 BXGD006880 Adenomatous goiter Neoplasms; Endocrine System Diseases
C0332909 BXGD006910 Congenital unilateral absence
C0334121 BXGD006996 Inflammatory Myofibroblastic Tumor Pathological Conditions, Signs and Symptoms
C0334299 BXGD007027 Carcinoid tumor no ICD-O subtype Neoplasms
C0334371 BXGD007049 Secretory breast carcinoma Neoplasms; Skin and Connective Tissue Diseases
C0334439 BXGD007069 Malignant desmoplastic melanoma Neoplasms
C0334595 BXGD007130 Ganglioneuromatosis Neoplasms
C0334607 BXGD007135 Psammomatous Meningioma Neoplasms; Nervous System 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
C0342208 BXGD007445 Multinodular goiter Neoplasms; Endocrine System Diseases
C0342443 BXGD007481 Adrenal Cushing's syndrome Endocrine System Diseases
C0343640 BXGD007635 African Burkitt's lymphoma Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases
C0345237 BXGD007720 Short segment Hirschsprung's disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
C0345240 BXGD007721 Total intestinal aganglionosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
C0345244 BXGD007722 Neuronal intestinal dysplasia Digestive System Diseases
C0345245 BXGD007723 Hyperganglionosis
C0345904 BXGD007745 Malignant neoplasm of liver Digestive System Diseases; Neoplasms
C0346153 BXGD007781 Breast Cancer, Familial Neoplasms; Skin and Connective Tissue Diseases
C0346398 BXGD007822 Mixed follicular and papillary thyroid carcinoma
C0346647 BXGD007832 Malignant neoplasm of pancreas Digestive System Diseases; Neoplasms; Endocrine System Diseases
C0346957 BXGD007836 Disseminated Malignant Neoplasm Neoplasms
C0348898 BXGD007884 Irritable bowel syndrome with diarrhea Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C0349530 BXGD007916 Early gastric cancer Digestive System Diseases; Neoplasms
C0349588 BXGD007933 Short stature
C0349639 BXGD007943 Juvenile Myelomonocytic Leukemia Neoplasms; Hemic and Lymphatic Diseases
C0376358 BXGD007992 Malignant neoplasm of prostate Neoplasms; Male Urogenital Diseases
C0376480 BXGD007998 Gingival Overgrowth Stomatognathic Diseases
C0376544 BXGD008001 Hematopoietic Neoplasms Neoplasms; Hemic and Lymphatic Diseases
C0376545 BXGD008002 Hematologic Neoplasms Neoplasms; Hemic and Lymphatic Diseases
C0393734 BXGD008131 Complex Partial Status Epilepticus Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0398597 BXGD008198 Histiocytic syndrome Immune System Diseases; Hemic and Lymphatic Diseases
C0398738 BXGD008222 Leukocyte adhesion deficiency type 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases
C0403622 BXGD008299 Primary vesicoureteric reflux Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0406810 BXGD008374 Carney Complex Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Cardiovascular Diseases
C0423110 BXGD008471 Downward slant of palpebral fissure
C0424295 BXGD008524 Hyperactive behavior Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0426576 BXGD008571 Gastrointestinal symptom Pathological Conditions, Signs and Symptoms
C0431478 BXGD008692 Posteriorly rotated ear
C0431564 BXGD008694 Lobulated tongue
C0432291 BXGD008767 Mandibuloacral dysostosis Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0432306 BXGD008770 Ichthyosis Bullosa of Siemens Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
C0442874 BXGD008814 Neuropathy Nervous System Diseases
C0474808 BXGD008959 Follicular neoplasm Neoplasms
C0476073 BXGD008976 Papillary neoplasm Neoplasms
C0476089 BXGD008977 Endometrial Carcinoma Neoplasms; Female Urogenital Diseases and Pregnancy Complications
C0494165 BXGD009022 Secondary malignant neoplasm of liver Digestive System Diseases; Neoplasms
C0497156 BXGD009053 Lymphadenopathy Hemic and Lymphatic Diseases
C0497550 BXGD009066 Benign neurologic neoplasms Neoplasms; Nervous System Diseases
C0520680 BXGD009102 Sleep Apnea, Central Respiratory Tract Diseases; Nervous System Diseases
C0521158 BXGD009130 Recurrent tumor
C0521670 BXGD009160 Cranial nerve compression Nervous System Diseases; Wounds and Injuries
C0522357 BXGD009202 Vertigo, Paroxysmal Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0522631 BXGD009205 Acute myeloid leukemia, minimal differentiation Neoplasms
C0524620 BXGD009236 Metabolic Syndrome X Nutritional and Metabolic Diseases
C0542519 BXGD009279 Congenital absence of kidney Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0545074 BXGD009324 Myxoid/Round Cell Liposarcoma Neoplasms
C0546275 BXGD009332 Hypoganglionosis
C0549473 BXGD009384 Thyroid carcinoma Neoplasms; Endocrine System Diseases
C0553580 BXGD009399 Ewings sarcoma Neoplasms
C0553723 BXGD009416 Squamous cell carcinoma of skin Neoplasms; Skin and Connective Tissue Diseases
C0557874 BXGD009444 Global developmental delay
C0585442 BXGD009593 Osteosarcoma of bone Neoplasms
C0596263 BXGD009639 Carcinogenesis Pathological Conditions, Signs and Symptoms; Neoplasms
C0598766 BXGD009669 Leukemogenesis Pathological Conditions, Signs and Symptoms; Neoplasms
C0598935 BXGD009674 Tumor Initiation Pathological Conditions, Signs and Symptoms; Neoplasms
C0600139 BXGD009695 Prostate carcinoma Neoplasms; Male Urogenital Diseases
C0677607 BXGD009721 Hashimoto Disease Endocrine 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
C0677948 BXGD009739 Stage II 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
C0686619 BXGD009835 Secondary malignant neoplasm of lymph node Pathological Conditions, Signs and Symptoms; Neoplasms
C0687150 BXGD009842 Parathyroid Gland Adenocarcinoma Neoplasms; Endocrine System Diseases
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
C0700095 BXGD009875 Central neuroblastoma Neoplasms; Nervous System Diseases
C0700292 BXGD009884 Hypoxemia Pathological Conditions, Signs and Symptoms
C0700639 BXGD009899 Pyloric Stenosis, Hypertrophic Digestive System Diseases
C0730303 BXGD009950 Capillary hemangioma of retina Neoplasms; Cardiovascular Diseases
C0740340 BXGD009978 Amyloidosis, Familial Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases
C0741899 BXGD010042 Poorly differentiated carcinoma
C0749424 BXGD010217 Thyroid Hurthle Cell Carcinoma Neoplasms; Endocrine System Diseases
C0749474 BXGD010220 thyroid nodule solitary Neoplasms; Endocrine System Diseases
C0750952 BXGD010263 Biliary Tract Cancer Digestive System Diseases; Neoplasms
C0751522 BXGD010488 Status Epilepticus, Subclinical Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751523 BXGD010489 Non-Convulsive Status Epilepticus Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751524 BXGD010490 Simple Partial Status Epilepticus Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C0751559 BXGD010500 Pulsatile Tinnitus Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C0796033 BXGD010785 MARDEN-WALKER SYNDROME Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
C0796070 BXGD010792 MICROPHTHALMIA, SYNDROMIC 7 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Skin and Connective Tissue Diseases
C0812413 BXGD010847 Malignant Pleural Mesothelioma Neoplasms; Respiratory Tract Diseases
C0853877 BXGD010981 Fistula of genitourinary tract Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C0853879 BXGD010982 Invasive carcinoma of breast Neoplasms; Skin and Connective Tissue Diseases
C0854914 BXGD011048 Retinoblastoma bilateral Neoplasms; Eye Diseases
C0878500 BXGD011365 Intraepithelial Neoplasia Neoplasms
C0878627 BXGD011376 Mucosal neuromas Neoplasms
C0917805 BXGD011414 Transient Cerebral Ischemia Nervous System Diseases; Cardiovascular Diseases
C0919267 BXGD011426 ovarian neoplasm Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C0920350 BXGD011466 Autoimmune thyroiditis Immune System Diseases; Endocrine System Diseases
C0949541 BXGD011578 Hurthle Cell Tumor Neoplasms
C1096168 BXGD011606 Chromosome 17 trisomy Pathological Conditions, Signs and Symptoms
C1140680 BXGD011718 Malignant neoplasm of ovary Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases
C1168401 BXGD011792 Squamous cell carcinoma of the head and neck Neoplasms
C1176475 BXGD011798 Ductal Carcinoma Neoplasms
C1257840 BXGD011809 Aganglionosis, Rectosigmoid Colon Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
C1257877 BXGD011812 Pheochromocytoma, Extra-Adrenal Neoplasms
C1257915 BXGD011813 Intestinal Polyposis Digestive System Diseases
C1261473 BXGD011855 Sarcoma Neoplasms
C1262477 BXGD011882 Weight decreased Pathological Conditions, Signs and Symptoms
C1266050 BXGD011945 Poorly Differentiated Thyroid Carcinoma Neoplasms; Endocrine System Diseases
C1266051 BXGD011946 Papillary microcarcinoma
C1266088 BXGD011953 Adenocarcinoma with neuroendocrine differentiation Neoplasms
C1269955 BXGD012005 Tumor Cell Invasion
C1275278 BXGD012074 Extraskeletal Myxoid Chondrosarcoma Neoplasms
C1275808 BXGD012094 Congenital central hypoventilation Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases
C1292778 BXGD012237 Chronic myeloproliferative disorder Neoplasms; Hemic and Lymphatic Diseases
C1301194 BXGD012284 Salivary duct carcinoma Neoplasms
C1306459 BXGD012361 Primary malignant neoplasm Neoplasms
C1306460 BXGD012362 Primary malignant neoplasm of lung Neoplasms; Respiratory Tract Diseases
C1319315 BXGD012415 Adenocarcinoma of large intestine Digestive System Diseases; Neoplasms
C1321756 BXGD012440 Achalasia
C1332206 BXGD012504 Adult Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332979 BXGD012571 Childhood Lymphoma Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases
C1332986 BXGD012574 Childhood Osteosarcoma Neoplasms
C1333015 BXGD012581 Childhood Kidney Wilms Tumor Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1333280 BXGD012609 Desmoplastic melanoma Neoplasms; Skin and Connective Tissue Diseases
C1333600 BXGD012636 Hereditary Malignant Neoplasm Neoplasms
C1333944 BXGD012657 Paraganglioma of head and neck Neoplasms
C1333993 BXGD012673 hereditary paraganglioma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C1334953 BXGD012746 Neuroblastic tumors Neoplasms
C1336052 BXGD012826 Spindle Cell Neoplasm
C1336082 BXGD012832 Thymic Squamous Cell Carcinoma Neoplasms; Hemic and Lymphatic Diseases
C1336750 BXGD012861 Thyroid Gland Oncocytic Adenoma Neoplasms; Endocrine System Diseases
C1336751 BXGD012862 Thyroid Hyalinizing Trabecular Adenoma Neoplasms; Endocrine System Diseases
C1337011 BXGD012874 Well Differentiated Pancreatic Endocrine Tumor Digestive System Diseases; Neoplasms; Endocrine System Diseases
C1337013 BXGD012876 Differentiated Thyroid Gland Carcinoma
C1384514 BXGD012940 Conn Syndrome Endocrine System Diseases
C1384666 BXGD012948 hearing impairment Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C1387805 BXGD012958 Episodic paroxysmal anxiety Behavior and Behavior Mechanisms
C1402294 BXGD013016 Primary Lesion
C1449563 BXGD013086 Cardiomyopathy, Familial Idiopathic Cardiovascular Diseases
C1458155 BXGD013136 Mammary Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C1510472 BXGD013170 Drug Dependence Chemically-Induced Disorders; Mental Disorders
C1510475 BXGD013171 Diverticulosis Pathological Conditions, Signs and Symptoms; Digestive System Diseases
C1511789 BXGD013183 Desmoplastic
C1519383 BXGD013237 Smoking Behaviors Behavior and Behavior Mechanisms
C1519670 BXGD013241 Tumor Angiogenesis Pathological Conditions, Signs and Symptoms
C1527344 BXGD013275 Dysphonia Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases; Otorhinolaryngologic Diseases
C1527349 BXGD013277 Ductal Breast Carcinoma Neoplasms
C1608408 BXGD013434 Malignant transformation
C1609433 BXGD013438 Congenital absence of kidneys syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1611743 BXGD013456 Familial (FPAH)
C1619700 BXGD013459 RENAL ADYSPLASIA Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1621958 BXGD013468 Glioblastoma Multiforme Neoplasms
C1654637 BXGD013484 androgen independent prostate cancer
C1704374 BXGD013550 Carcinoma of Endocrine Gland Neoplasms; Endocrine System Diseases
C1704981 BXGD013567 Hyperparathyroidism-Jaw Tumor Syndrome Neoplasms; Musculoskeletal Diseases; Endocrine System Diseases; Stomatognathic Diseases
C1705254 BXGD013568 Neonatal Deformity Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C1707446 BXGD013587 Columnar Cell Hyperplasia of the Breast
C1708353 BXGD013599 Hereditary Paraganglioma-Pheochromocytoma Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C1709457 BXGD013625 Papillary Thyroid Microcarcinoma Neoplasms; Endocrine System Diseases
C1800706 BXGD013755 Idiopathic Pulmonary Fibrosis Respiratory Tract Diseases
C1832160 BXGD013803 Abnormality of temperature regulation
C1832589 BXGD013857 Neuronal Intestinal Dysplasia, Type B Digestive System Diseases; Nervous System Diseases
C1832661 BXGD013866 ANOPHTHALMIA AND PULMONARY HYPOPLASIA Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases; Respiratory Tract Diseases
C1833921 BXGD013946 Familial medullary thyroid carcinoma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
C1833929 BXGD013947 THYROID CARCINOMA, SPORADIC MEDULLARY
C1836543 BXGD014130 Thick vermilion border
C1836996 BXGD014183 Disproportionate tall stature
C1837249 BXGD014210 Malformations of Cortical Development, Group II Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C1837404 BXGD014229 High, narrow palate
C1837475 BXGD014236 Insulin-Like Growth Factor I Deficiency Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases
C1839259 BXGD014363 Bulbo-Spinal Atrophy, X-Linked Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C1839739 BXGD014400 Thick lower lip vermilion
C1842876 BXGD014542 Depressed nasal ridge
C1842981 BXGD014547 NEUROTICISM Behavior and Behavior Mechanisms
C1844820 BXGD014681 Range of joint movement increased
C1845667 BXGD014756 RETINITIS PIGMENTOSA 3 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases
C1847800 BXGD014889 Waardenburg Syndrome Type 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C1848519 BXGD014932 WAARDENBURG SYNDROME, TYPE 4A Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
C1851585 BXGD015222 MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA Hemic and Lymphatic Diseases
C1853487 BXGD015340 Thick eyebrow
C1857171 BXGD015680 Episodic hyperhidrosis Skin and Connective Tissue Diseases
C1857175 BXGD015681 Episodic hypertension Cardiovascular Diseases
C1857276 BXGD015688 Trichohepatoenteric Syndrome Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Skin and Connective Tissue Diseases
C1858120 BXGD015774 Generalized hypotonia Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C1858430 BXGD015792 Death in infancy
C1859049 BXGD015846 CCHS WITH HIRSCHSPRUNG DISEASE Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases; Nervous System Diseases
C1865279 BXGD016303 Fetal polyuria
C1865292 BXGD016306 Nonketotic hypoglycemia Nutritional and Metabolic Diseases
C1867403 BXGD016450 Pyloric Stenosis, Infantile Hypertrophic 1 Digestive System Diseases
C1867873 BXGD016473 Failure to thrive in infancy
C1868393 BXGD016498 Elevated urinary epinephrine
C1868394 BXGD016499 Elevated calcitonin
C1879321 BXGD016572 Acute Myeloid Leukemia (AML-M2) Neoplasms
C1968949 BXGD016744 Cakut Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C1970712 BXGD016842 Multiple Endocrine Neoplasia, Type IV Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
C2239176 BXGD016965 Liver carcinoma Digestive System Diseases; Neoplasms
C2919142 BXGD017867 Short Stature, CTCAE
C2930839 BXGD017902 Bilateral pheochromocytoma and islet cell adenoma of the pancreas Digestive System Diseases; Neoplasms; Endocrine System Diseases
C2931189 BXGD017972 Neural crest tumor Neoplasms; Endocrine System Diseases
C2931367 BXGD018010 Thyroid cancer, follicular Neoplasms
C2937358 BXGD018159 Cerebral Hemorrhage Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases
C2938924 BXGD018167 Oestrogen receptor positive breast cancer
C2939419 BXGD018178 Secondary Neoplasm Pathological Conditions, Signs and Symptoms; Neoplasms
C2945759 BXGD018189 aggressive cancer
C2985280 BXGD018223 Blood Protein Measurement
C2986682 BXGD018238 Locally Recurrent Malignant Neoplasm
C3146252 BXGD018261 Stage II Colorectal Cancer AJCC v7
C3146257 BXGD018265 Stage II Colon Cancer AJCC v7
C3160712 BXGD018467 Palpitations, CTCAE
C3203358 BXGD018558 Hypoventilation Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C3266262 BXGD018600 Multiple Chronic Conditions Pathological Conditions, Signs and Symptoms
C3266898 BXGD018606 Waardenburg Syndrome Congenital, Hereditary, and Neonatal Diseases and Abnormalities
C3267007 BXGD018609 Hypercalcitoninaemia Nutritional and Metabolic Diseases
C3495676 BXGD019000 Anorectal Malformations Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
C3501843 BXGD019027 Nonmedullary Thyroid Carcinoma Neoplasms; Endocrine System Diseases
C3501844 BXGD019028 Familial Nonmedullary Thyroid Cancer Neoplasms; Endocrine System 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
C3539878 BXGD019087 Triple Negative Breast Neoplasms Neoplasms; Skin and Connective Tissue Diseases
C3544229 BXGD019111 Congenital intestinal obstruction
C3554617 BXGD019228 Adducted thumb Musculoskeletal Diseases
C3649644 BXGD019251 Congenital condition
C3661523 BXGD019265 Congenital Intestinal Aganglionosis Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases
C3665346 BXGD019278 Unspecified visual loss Pathological Conditions, Signs and Symptoms; Eye Diseases
C3714651 BXGD019423 Follicular Variant Thyroid Gland Papillary Carcinoma Neoplasms; Endocrine System Diseases
C3714756 BXGD019429 Intellectual Disability Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms
C3805839 BXGD019490 Central hypoventilation Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases
C3805845 BXGD019491 Cutaneous lichen amyloidosis
C3808022 BXGD019536 Episodic abdominal pain Pathological Conditions, Signs and Symptoms
C3808046 BXGD019538 Breathing dysregulation
C3812899 BXGD019667 Papillary carcinoma of the breast Neoplasms
C3875007 BXGD019869 Nodular thyroid disease Endocrine System Diseases
C3888239 BXGD019962 HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1
C3888391 BXGD019969 Nonnuclear polymorphic congenital cataract
C3896673 BXGD020041 Familial Nonmedullary Thyroid Gland Carcinoma
C3899155 BXGD020075 hereditary neuroblastoma Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C3900101 BXGD020109 Adult Germ Cell Tumor Neoplasms
C4016285 BXGD020301 MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITHOUT PHEOCHROMOCYTOMA
C4016286 BXGD020302 MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIA, WITH HIRSCHSPRUNG DISEASE
C4020735 BXGD020475 Elevated urinary vanillylmandelic acid
C4021020 BXGD020521 Non-midline cleft lip Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
C4022998 BXGD021058 Arachnoid hemangiomatosis Neoplasms
C4023099 BXGD021105 Elevated urinary dopamine
C4025250 BXGD021605 Abnormal sacrum morphology
C4025594 BXGD021683 Positive regitine blocking test
C4025626 BXGD021701 Elevated urinary norepinephrine
C4025651 BXGD021712 Increased circulating cortisol level
C4025761 BXGD021782 Abnormality of the integument
C4025900 BXGD021855 Abnormality of female internal genitalia
C4042906 BXGD021883 Mammary Analogue Secretory Carcinoma Neoplasms
C4048306 BXGD021902 Multiple endocrine neoplasia Type 2 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Endocrine System Diseases
C4049711 BXGD021949 Lepidic Predominant Adenocarcinoma Neoplasms
C4049796 BXGD021951 Abnormality of cardiovascular system morphology Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C4086151 BXGD022122 Childhood Anaplastic Ependymoma Neoplasms
C4086165 BXGD022126 Childhood Neuroblastoma Neoplasms
C4086178 BXGD022128 Childhood Thyroid Gland Papillary Carcinoma Neoplasms; Endocrine System Diseases
C4282128 BXGD022420 PATENT DUCTUS ARTERIOSUS 1 Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
C4287590 BXGD022470 Thyroid Gland Noninvasive Follicular Neoplasm with Papillary-Like Nuclear Features Neoplasms; Endocrine System Diseases
C4293671 BXGD022509 Abnormality of enteric ganglion morphology
C4293708 BXGD022515 Recurrent paroxysmal headache Pathological Conditions, Signs and Symptoms
C4316788 BXGD022697 Abnormality of the intestine
C4317009 BXGD022717 Diverticular Diseases Digestive System Diseases
C4324656 BXGD022775 Non-squamous non-small cell lung cancer Neoplasms; Respiratory Tract Diseases
C4511687 BXGD023010 Pancreatic Intraductal Papillary Mucinous Neoplasm Digestive System Diseases; Neoplasms; Endocrine System Diseases
C4520821 BXGD023039 Stage 0 Breast Cancer AJCC v6 and v7 Neoplasms; Skin and Connective Tissue Diseases
C4521042 BXGD023055 Complete Trisomy 21 Syndrome Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
C4523846 BXGD023079 MSI-high
C4525119 BXGD023118 Stage II Colon Cancer AJCC v8
C4551506 BXGD023326 Paroxysmal Nonkinesigenic Dyskinesia 1 Pathological Conditions, Signs and Symptoms; Nervous System Diseases
C4551683 BXGD023389 Adrenal Gland Pheochromocytoma Neoplasms; Endocrine System Diseases
C4551686 BXGD023391 Malignant neoplasm of soft tissue Neoplasms
C4551858 BXGD023425 Vesicoureteral Reflux 1 Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases
C4551961 BXGD023451 Familial Isolated Hyperparathyroidism Endocrine System Diseases
C4721444 BXGD023742 Burkitt Leukemia Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases
C4721453 BXGD023744 Peripheral Nervous System Diseases Nervous System 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
C4722172 BXGD023791 Primary differentiated carcinoma of thyroid gland
C4722518 BXGD023806 Triple-Negative Breast Carcinoma Neoplasms; Skin and Connective Tissue Diseases
C4727087 BXGD023856 Metastatic Lung Carcinoma
C4733092 BXGD023907 estrogen receptor-negative breast cancer
C4733333 BXGD023920 familial non-medullary thyroid cancer Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms
C4733537 BXGD023924 recurrent medullary thyroid cancer Neoplasms; Endocrine System Diseases
C4744444 BXGD023941 Metastatic Lung Adenocarcinoma Neoplasms
Target protein-related  compounds
Compounds
BXGC Id Compound Name Strcuture Molecular Weight
BXGC0002586 Calcium 40.08
BXGC0002605 Adenosine 267.24
BXGC0003705 Chloride 35.45
BXGC0005683 Quercetin 302.24
BXGC0006193 Ellagic acid 302.19
BXGC0006368 Formic acid 46.03
BXGC0012352 Chelerythrine 348.12
BXGC0013109 4-[2-(3,5-Dihydroxyphenyl)Ethenyl]Benzene-1,2-Diol 244.07
BXGC0016891 Nortriptyline 263.17
BXGC0023872 Adenine 135.05
BXGC0024261 Adenosine Phosphate 347.06
BXGC0042376 Picropodophyllotoxin 414.13
BXGC0044857 Sp-600125 220.06
BXGC0045254 Sb-202190 331.11
BXGC0047692 Gefitinib 446.15
BXGC0049447 acetate 59.01
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