| C0000744 |
BXGD000006 |
Abetalipoproteinemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0000772 |
BXGD000009 |
Multiple congenital anomalies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0001418 |
BXGD000050 |
Adenocarcinoma |
Neoplasms |
| C0001807 |
BXGD000077 |
Aggressive behavior |
Behavior and Behavior Mechanisms |
| C0002395 |
BXGD000111 |
Alzheimer's Disease |
Nervous System Diseases; Mental Disorders |
| C0002418 |
BXGD000112 |
Amblyopia |
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases |
| C0002894 |
BXGD000151 |
Refractory anaemia with excess blasts |
Hemic and Lymphatic Diseases |
| C0003467 |
BXGD000194 |
Anxiety |
Behavior and Behavior Mechanisms |
| C0003850 |
BXGD000225 |
Arteriosclerosis |
Cardiovascular Diseases |
| C0003873 |
BXGD000236 |
Rheumatoid Arthritis |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0004153 |
BXGD000260 |
Atherosclerosis |
Cardiovascular Diseases |
| C0004352 |
BXGD000269 |
Autistic Disorder |
Mental Disorders |
| C0004403 |
BXGD000272 |
Autosome Abnormalities |
Pathological Conditions, Signs and Symptoms |
| 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 |
| C0005699 |
BXGD000325 |
Blast Phase |
Pathological Conditions, Signs and Symptoms; Neoplasms; Hemic and Lymphatic Diseases |
| C0005741 |
BXGD000328 |
Blepharitis |
Eye Diseases |
| C0005744 |
BXGD000330 |
Blepharophimosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0005745 |
BXGD000331 |
Blepharoptosis |
Eye Diseases |
| C0005779 |
BXGD000336 |
Blood Coagulation Disorders |
Hemic and Lymphatic Diseases |
| C0005890 |
BXGD000345 |
Body Height |
|
| C0006118 |
BXGD000372 |
Brain Neoplasms |
Neoplasms; Nervous System Diseases |
| C0006142 |
BXGD000374 |
Malignant neoplasm of breast |
Neoplasms; Skin and Connective Tissue Diseases |
| C0006287 |
BXGD000390 |
Bronchopulmonary Dysplasia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases |
| C0006413 |
BXGD000397 |
Burkitt Lymphoma |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0006826 |
BXGD000408 |
Malignant Neoplasms |
Neoplasms |
| C0007097 |
BXGD000424 |
Carcinoma |
Neoplasms |
| C0007102 |
BXGD000425 |
Malignant tumor of colon |
Digestive System Diseases; Neoplasms |
| C0007107 |
BXGD000428 |
Malignant neoplasm of larynx |
Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C0007131 |
BXGD000441 |
Non-Small Cell Lung Carcinoma |
Neoplasms; Respiratory Tract Diseases |
| C0007134 |
BXGD000443 |
Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0007138 |
BXGD000446 |
Carcinoma, Transitional Cell |
Neoplasms |
| C0007194 |
BXGD000452 |
Hypertrophic Cardiomyopathy |
Cardiovascular Diseases |
| C0007222 |
BXGD000454 |
Cardiovascular Diseases |
Cardiovascular Diseases |
| C0007785 |
BXGD000485 |
Cerebral Infarction |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0007786 |
BXGD000486 |
Brain Ischemia |
Nervous System Diseases; Cardiovascular Diseases |
| C0007873 |
BXGD000500 |
Uterine Cervical Neoplasm |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications |
| C0008073 |
BXGD000518 |
Developmental Disabilities |
Mental Disorders |
| C0008297 |
BXGD000522 |
Choanal Atresia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C0008476 |
BXGD000543 |
Chondromatosis, Synovial |
Musculoskeletal Diseases |
| C0008479 |
BXGD000544 |
Chondrosarcoma |
Neoplasms |
| C0008625 |
BXGD000558 |
Chromosome Aberrations |
Pathological Conditions, Signs and Symptoms |
| 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 |
| C0009402 |
BXGD000605 |
Colorectal Carcinoma |
Digestive System Diseases; Neoplasms |
| C0010054 |
BXGD000647 |
Coronary Arteriosclerosis |
Cardiovascular Diseases |
| C0010417 |
BXGD000670 |
Cryptorchidism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Male Urogenital Diseases; Endocrine System Diseases |
| C0011168 |
BXGD000700 |
Deglutition Disorders |
Digestive System Diseases; Otorhinolaryngologic Diseases |
| 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 |
| C0011881 |
BXGD000760 |
Diabetic Nephropathy |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Endocrine System Diseases |
| C0013080 |
BXGD000797 |
Down Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0013336 |
BXGD000815 |
Dwarfism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0014457 |
BXGD000915 |
Eosinophilia |
Hemic and Lymphatic Diseases |
| C0014544 |
BXGD000926 |
Epilepsy |
Nervous System Diseases |
| C0014772 |
BXGD000948 |
Red Blood Cell Count measurement |
|
| C0015230 |
BXGD000969 |
Exanthema |
Skin and Connective Tissue Diseases |
| C0015544 |
BXGD001003 |
Failure to Thrive |
Pathological Conditions, Signs and Symptoms |
| C0015625 |
BXGD001006 |
Fanconi Anemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |
| C0015732 |
BXGD001018 |
Fecal Incontinence |
Digestive System Diseases |
| C0015923 |
BXGD001023 |
Fetal Alcohol Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Chemically-Induced Disorders |
| C0015934 |
BXGD001026 |
Fetal Growth Retardation |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications |
| C0016057 |
BXGD001042 |
Fibrosarcoma |
Neoplasms |
| C0016842 |
BXGD001083 |
Congenital pectus excavatum |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0017168 |
BXGD001101 |
Gastroesophageal reflux disease |
Digestive System Diseases |
| C0017601 |
BXGD001125 |
Glaucoma |
Eye Diseases |
| C0017636 |
BXGD001131 |
Glioblastoma |
Neoplasms |
| C0017638 |
BXGD001132 |
Glioma |
Neoplasms |
| C0018133 |
BXGD001176 |
Graft-vs-Host Disease |
Immune System Diseases |
| C0018203 |
BXGD001184 |
Chronic granulomatous disease |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases |
| 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 |
| C0018801 |
BXGD001226 |
Heart failure |
Cardiovascular Diseases |
| C0018802 |
BXGD001227 |
Congestive heart failure |
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 |
| C0018939 |
BXGD001253 |
Hematological Disease |
Hemic and Lymphatic Diseases |
| C0019163 |
BXGD001295 |
Hepatitis B |
Digestive System Diseases; Infections |
| C0019572 |
BXGD001338 |
Hirsutism |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C0019693 |
BXGD001346 |
HIV Infections |
Infections; Immune System Diseases |
| C0019829 |
BXGD001350 |
Hodgkin Disease |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0020445 |
BXGD001386 |
Hypercholesterolemia, Familial |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0020456 |
BXGD001392 |
Hyperglycemia |
Nutritional and Metabolic Diseases |
| C0020534 |
BXGD001421 |
Orbital separation excessive |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0020538 |
BXGD001422 |
Hypertensive disease |
Cardiovascular Diseases |
| C0020555 |
BXGD001431 |
Hypertrichosis |
Skin and Connective Tissue Diseases |
| C0021051 |
BXGD001475 |
Immunologic Deficiency Syndromes |
Immune System Diseases |
| C0022658 |
BXGD001570 |
Kidney Diseases |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0022738 |
BXGD001582 |
Klippel-Feil Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0023418 |
BXGD001642 |
leukemia |
Neoplasms |
| C0023434 |
BXGD001643 |
Chronic Lymphocytic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023440 |
BXGD001646 |
Acute Erythroblastic Leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C0023443 |
BXGD001648 |
Hairy Cell Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023448 |
BXGD001649 |
Lymphoid 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 |
| C0023453 |
BXGD001652 |
L2 Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023462 |
BXGD001654 |
Acute Megakaryocytic Leukemias |
Neoplasms |
| C0023464 |
BXGD001655 |
Acute biphenotypic leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023465 |
BXGD001656 |
Acute monocytic leukemia |
Neoplasms |
| C0023466 |
BXGD001657 |
Leukemia, Monocytic, Chronic |
Neoplasms |
| C0023467 |
BXGD001658 |
Leukemia, Myelocytic, Acute |
Neoplasms |
| C0023470 |
BXGD001659 |
Myeloid Leukemia |
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 |
| C0023485 |
BXGD001667 |
Precursor B-Cell Lymphoblastic Leukemia-Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023487 |
BXGD001669 |
Acute Promyelocytic Leukemia |
Neoplasms |
| C0023492 |
BXGD001671 |
Leukemia, T-Cell |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023493 |
BXGD001672 |
Adult T-Cell Lymphoma/Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0023518 |
BXGD001677 |
Leukocytosis |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0024117 |
BXGD001734 |
Chronic Obstructive Airway Disease |
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 |
| C0024301 |
BXGD001759 |
Lymphoma, Follicular |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024305 |
BXGD001763 |
Lymphoma, Non-Hodgkin |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0024623 |
BXGD001791 |
Malignant neoplasm of stomach |
Digestive System Diseases; Neoplasms |
| C0025202 |
BXGD001832 |
melanoma |
Neoplasms |
| C0025286 |
BXGD001850 |
Meningioma |
Neoplasms; Nervous System Diseases |
| C0025517 |
BXGD001875 |
Metabolic Diseases |
Nutritional and Metabolic Diseases |
| C0025958 |
BXGD001882 |
Microcephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases |
| C0025990 |
BXGD001884 |
Micrognathism |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases |
| C0025995 |
BXGD001885 |
Micromelia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| 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 |
| C0026769 |
BXGD001930 |
Multiple Sclerosis |
Immune System Diseases; Nervous System 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 |
|
| C0026998 |
BXGD001959 |
Acute Myeloid Leukemia, M1 |
Neoplasms |
| C0027019 |
BXGD001961 |
Myelomonocytic leukemia |
Neoplasms |
| C0027022 |
BXGD001962 |
Myeloproliferative disease |
Hemic and Lymphatic Diseases |
| C0027051 |
BXGD001963 |
Myocardial Infarction |
Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases |
| C0027092 |
BXGD001971 |
Myopia |
Eye Diseases |
| C0027533 |
BXGD001995 |
Neck Neoplasms |
Neoplasms |
| C0027627 |
BXGD002006 |
Neoplasm Metastasis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0027651 |
BXGD002009 |
Neoplasms |
Neoplasms |
| C0027708 |
BXGD002025 |
Nephroblastoma |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0027819 |
BXGD002043 |
Neuroblastoma |
Neoplasms |
| C0028738 |
BXGD002081 |
Nystagmus |
Eye Diseases; Nervous System Diseases |
| C0029427 |
BXGD002144 |
Synovial osteochondromatosis |
Musculoskeletal Diseases |
| C0029463 |
BXGD002160 |
Osteosarcoma |
Neoplasms |
| C0030297 |
BXGD002204 |
Pancreatic Neoplasm |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0030312 |
BXGD002207 |
Pancytopenia |
Hemic and Lymphatic Diseases |
| C0030567 |
BXGD002240 |
Parkinson Disease |
Nervous System Diseases |
| C0033377 |
BXGD002406 |
Ptosis |
Pathological Conditions, Signs and Symptoms |
| C0033578 |
BXGD002408 |
Prostatic Neoplasms |
Neoplasms; Male Urogenital Diseases |
| C0034012 |
BXGD002449 |
Delayed Puberty |
Endocrine System Diseases |
| C0034194 |
BXGD002472 |
Pyloric Stenosis |
Digestive System Diseases |
| C0035204 |
BXGD002511 |
Respiration Disorders |
Respiratory Tract Diseases |
| C0035242 |
BXGD002521 |
Respiratory Tract Diseases |
Respiratory Tract Diseases |
| C0036341 |
BXGD002600 |
Schizophrenia |
Mental Disorders |
| C0036421 |
BXGD002613 |
Systemic Scleroderma |
Skin and Connective Tissue Diseases |
| C0036572 |
BXGD002625 |
Seizures |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0036857 |
BXGD002638 |
Severe intellectual disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0037274 |
BXGD002676 |
Dermatologic disorders |
Skin and Connective Tissue Diseases |
| C0037317 |
BXGD002689 |
Sleep disturbances |
Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0037822 |
BXGD002706 |
Speech Disorders |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0038271 |
BXGD002742 |
Stereotyped Behavior |
Behavior and Behavior Mechanisms |
| C0038273 |
BXGD002743 |
Stereotypic Movement Disorder |
Mental Disorders |
| C0038356 |
BXGD002747 |
Stomach Neoplasms |
Digestive System Diseases; Neoplasms |
| C0038379 |
BXGD002752 |
Strabismus |
Eye Diseases; Nervous System Diseases |
| C0041696 |
BXGD002932 |
Unipolar Depression |
Mental Disorders |
| C0042580 |
BXGD002992 |
Vesico-Ureteral Reflux |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0042961 |
BXGD003017 |
Intestinal Volvulus |
Pathological Conditions, Signs and Symptoms; Digestive System Diseases |
| C0079731 |
BXGD003087 |
B-Cell Lymphomas |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079744 |
BXGD003090 |
Diffuse Large B-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079748 |
BXGD003094 |
Precursor cell lymphoblastic lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0079772 |
BXGD003099 |
T-Cell Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0085090 |
BXGD003122 |
Lymphoma, AIDS-Related |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0085096 |
BXGD003123 |
Peripheral Vascular Diseases |
Cardiovascular Diseases |
| C0085183 |
BXGD003139 |
Neoplasms, Second Primary |
Neoplasms |
| C0085281 |
BXGD003152 |
Addictive Behavior |
Behavior and Behavior Mechanisms |
| C0085669 |
BXGD003233 |
Acute leukemia |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0085702 |
BXGD003247 |
Monocytosis |
Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases |
| C0086543 |
BXGD003294 |
Cataract |
Eye Diseases |
| C0087031 |
BXGD003319 |
Juvenile-Onset Still Disease |
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases |
| C0149925 |
BXGD003387 |
Small cell carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0150080 |
BXGD003402 |
Social Communication Disorder |
Mental Disorders |
| C0151526 |
BXGD003432 |
Premature Birth |
Female Urogenital Diseases and Pregnancy Complications |
| C0151744 |
BXGD003469 |
Myocardial Ischemia |
Cardiovascular Diseases |
| C0151747 |
BXGD003471 |
Renal tubular disorder |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0152276 |
BXGD003581 |
Granulocytic Sarcoma |
Neoplasms |
| C0152415 |
BXGD003583 |
Ankyloglossia |
Stomatognathic Diseases |
| C0152421 |
BXGD003586 |
Macrotia |
|
| C0152423 |
BXGD003587 |
Congenital small ears |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Otorhinolaryngologic Diseases |
| C0158621 |
BXGD003893 |
Congenital subaortic stenosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases |
| C0158761 |
BXGD003905 |
Radioulnar Synostosis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0158945 |
BXGD003913 |
Congenital cytomegalovirus infection |
Infections |
| C0162298 |
BXGD003933 |
Joint stiffness |
Musculoskeletal Diseases |
| C0162557 |
BXGD003956 |
Liver Failure, Acute |
Digestive System Diseases |
| C0175754 |
BXGD004015 |
Agenesis of corpus callosum |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0178874 |
BXGD004037 |
Tumor Progression |
Pathological Conditions, Signs and Symptoms |
| C0205641 |
BXGD004093 |
Adenocarcinoma, Basal Cell |
Neoplasms |
| C0205642 |
BXGD004094 |
Adenocarcinoma, Oxyphilic |
Neoplasms |
| C0205643 |
BXGD004095 |
Carcinoma, Cribriform |
Neoplasms |
| C0205644 |
BXGD004096 |
Carcinoma, Granular Cell |
Neoplasms |
| C0205645 |
BXGD004097 |
Adenocarcinoma, Tubular |
Neoplasms |
| C0205647 |
BXGD004099 |
Follicular adenoma |
Neoplasms |
| C0206698 |
BXGD004248 |
Cholangiocarcinoma |
Neoplasms |
| C0220605 |
BXGD004294 |
Adult Non-Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0220612 |
BXGD004296 |
Childhood Non-Hodgkin Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0220615 |
BXGD004298 |
Adult Acute Myeloblastic Leukemia |
Neoplasms |
| C0220621 |
BXGD004300 |
Childhood Acute Myeloid Leukemia |
Neoplasms |
| C0220668 |
BXGD004317 |
Congenital contractural arachnodactyly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0221210 |
BXGD004406 |
Congenital malrotation of intestine |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Digestive System Diseases |
| C0221217 |
BXGD004408 |
Neck webbing |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0221354 |
BXGD004446 |
Frontal bossing |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0221356 |
BXGD004448 |
Brachycephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0221358 |
BXGD004450 |
Long narrow head |
|
| C0232466 |
BXGD004543 |
Feeding difficulties |
|
| C0232939 |
BXGD004568 |
Primary physiologic amenorrhea |
Pathological Conditions, Signs and Symptoms |
| C0233522 |
BXGD004585 |
Inappropriate behavior |
Behavior and Behavior Mechanisms |
| C0233794 |
BXGD004618 |
Memory impairment |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms |
| C0235833 |
BXGD004775 |
Congenital diaphragmatic hernia |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0235974 |
BXGD004796 |
Pancreatic carcinoma |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0239174 |
BXGD004969 |
Late tooth eruption |
|
| C0239234 |
BXGD004974 |
Low set ears |
|
| C0239479 |
BXGD004982 |
Round face |
|
| C0239676 |
BXGD004989 |
High forehead |
|
| C0240635 |
BXGD005047 |
Byzanthine arch palate |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Stomatognathic Diseases |
| C0242379 |
BXGD005157 |
Malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C0242596 |
BXGD005181 |
Neoplasm, Residual |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0262444 |
BXGD005244 |
Abnormality of the dentition |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases |
| C0262630 |
BXGD005262 |
Reduced concentration span |
Behavior and Behavior Mechanisms |
| C0263401 |
BXGD005298 |
Cutis marmorata |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Neoplasms; Skin and Connective Tissue Diseases; Cardiovascular Diseases; Wounds and Injuries |
| C0264303 |
BXGD005379 |
Laryngomalacia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C0265210 |
BXGD005463 |
Weaver syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Endocrine System Diseases |
| C0265219 |
BXGD005468 |
Miller Dieker syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0265535 |
BXGD005544 |
Trigonocephaly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0265660 |
BXGD005561 |
Syndactyly of the toes |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0266295 |
BXGD005645 |
Congenital hypoplasia of kidney |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0266383 |
BXGD005660 |
Uterine Anomalies |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0266435 |
BXGD005668 |
Congenital hypoplasia of penis |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0266544 |
BXGD005691 |
Microcornea |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C0270972 |
BXGD006147 |
Cornelia De Lange Syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0271007 |
BXGD006152 |
Phthisis bulbi |
Pathological Conditions, Signs and Symptoms; Eye Diseases |
| C0271561 |
BXGD006213 |
Somatotropin deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Endocrine System Diseases |
| C0278694 |
BXGD006564 |
Disseminated neuroblastoma |
Neoplasms |
| C0278704 |
BXGD006567 |
Malignant Childhood Neoplasm |
Neoplasms |
| C0278721 |
BXGD006572 |
Adult Lymphoblastic Lymphoma |
|
| C0278764 |
BXGD006581 |
Adult Burkitt Lymphoma |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0278877 |
BXGD006608 |
Adult Meningioma |
Neoplasms; Nervous System Diseases |
| C0278878 |
BXGD006609 |
Adult Glioblastoma |
Neoplasms |
| C0278879 |
BXGD006610 |
Childhood Burkitt Lymphoma |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0278996 |
BXGD006621 |
Malignant Head and Neck Neoplasm |
Neoplasms |
| C0279068 |
BXGD006624 |
Childhood Solid Neoplasm |
|
| C0279525 |
BXGD006627 |
Childhood Lymphoblastic Lymphoma |
|
| C0279582 |
BXGD006639 |
Childhood Burkitt Leukemia |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0279583 |
BXGD006640 |
Childhood T Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0279584 |
BXGD006641 |
Childhood B Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0279591 |
BXGD006642 |
Adult Burkitt Leukemia |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0279592 |
BXGD006643 |
Adult T Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0279593 |
BXGD006644 |
Adult B Acute Lymphoblastic Leukemia |
|
| C0279627 |
BXGD006658 |
Adult Acute Myelomonocytic Leukemia |
Neoplasms |
| C0279629 |
BXGD006660 |
Adult Acute Monoblastic Leukemia |
Neoplasms |
| C0279632 |
BXGD006663 |
Adult Acute Megakaryoblastic Leukemia |
Neoplasms |
| C0279644 |
BXGD006668 |
Childhood Acute Myelomonocytic Leukemia |
Neoplasms |
| C0279645 |
BXGD006669 |
Childhood Acute Monoblastic Leukemia |
|
| C0279646 |
BXGD006670 |
Childhood Acute Monocytic Leukemia |
Neoplasms |
| C0279650 |
BXGD006673 |
Childhood Acute Megakaryoblastic Leukemia |
Neoplasms |
| C0279702 |
BXGD006685 |
Conventional (Clear Cell) Renal Cell Carcinoma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0280099 |
BXGD006712 |
Adult Solid Neoplasm |
|
| C0280100 |
BXGD006713 |
Solid Neoplasm |
Neoplasms |
| C0280141 |
BXGD006716 |
Acute Undifferentiated Leukemia |
|
| C0280449 |
BXGD006746 |
secondary acute myeloid leukemia |
Neoplasms |
| C0280451 |
BXGD006747 |
de novo myelodysplastic syndromes |
Hemic and Lymphatic Diseases |
| C0280474 |
BXGD006748 |
Childhood Glioblastoma |
Neoplasms |
| C0280634 |
BXGD006753 |
Adult Acute Monocytic Leukemia |
Neoplasms |
| C0280745 |
BXGD006756 |
secondary myelodysplastic syndromes |
Hemic and Lymphatic Diseases |
| C0282160 |
BXGD006797 |
Aplasia Cutis Congenita |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0334634 |
BXGD007144 |
Malignant lymphoma, lymphocytic, intermediate differentiation, diffuse |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0334660 |
BXGD007148 |
Angioendotheliomatosis |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0338656 |
BXGD007211 |
Impaired cognition |
Mental Disorders |
| C0340375 |
BXGD007326 |
Subaortic stenosis |
Cardiovascular Diseases |
| C0342788 |
BXGD007552 |
Renal carnitine transport defect |
Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases; Nervous System Diseases; Cardiovascular Diseases |
| C0344482 |
BXGD007678 |
Hypoplasia of corpus callosum |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C0345354 |
BXGD007728 |
Radial polydactyly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0346153 |
BXGD007781 |
Breast Cancer, Familial |
Neoplasms; Skin and Connective Tissue Diseases |
| C0346647 |
BXGD007832 |
Malignant neoplasm of pancreas |
Digestive System Diseases; Neoplasms; Endocrine System Diseases |
| C0349588 |
BXGD007933 |
Short stature |
|
| C0349636 |
BXGD007941 |
Pre B-cell acute lymphoblastic leukemia |
|
| C0349637 |
BXGD007942 |
Common acute lymphoblastic leukemia |
|
| C0349639 |
BXGD007943 |
Juvenile Myelomonocytic Leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C0376358 |
BXGD007992 |
Malignant neoplasm of prostate |
Neoplasms; Male Urogenital Diseases |
| C0376544 |
BXGD008001 |
Hematopoietic Neoplasms |
Neoplasms; Hemic and Lymphatic Diseases |
| C0376545 |
BXGD008002 |
Hematologic Neoplasms |
Neoplasms; Hemic and Lymphatic Diseases |
| C0398791 |
BXGD008233 |
Nijmegen Breakage Syndrome |
Nutritional and Metabolic Diseases |
| C0401149 |
BXGD008273 |
Chronic constipation |
Pathological Conditions, Signs and Symptoms |
| C0406587 |
BXGD008355 |
Wrinkly skin syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0410652 |
BXGD008443 |
Cervical spine instability |
|
| C0423110 |
BXGD008471 |
Downward slant of palpebral fissure |
|
| C0423112 |
BXGD008472 |
Short palpebral fissure |
|
| C0423113 |
BXGD008473 |
Telecanthus |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0424295 |
BXGD008524 |
Hyperactive behavior |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0424503 |
BXGD008532 |
Dysmorphic facies |
|
| C0424605 |
BXGD008535 |
Developmental delay (disorder) |
Mental Disorders |
| C0426421 |
BXGD008561 |
Wide nose |
|
| C0426848 |
BXGD008590 |
Sacral dimple |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0426886 |
BXGD008594 |
Tapering fingers (finding) |
|
| C0427086 |
BXGD008605 |
Involuntary Movements |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C0431447 |
BXGD008690 |
Synophrys |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C0432072 |
BXGD008718 |
Dysmorphic features |
|
| C0432355 |
BXGD008780 |
Hypoplasia of nipple |
|
| C0432409 |
BXGD008786 |
Trisomy 11 |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C0454644 |
BXGD008850 |
Delayed speech and language development |
Behavior and Behavior Mechanisms |
| C0457334 |
BXGD008888 |
Acute monoblastic leukemia |
Neoplasms |
| C0497156 |
BXGD009053 |
Lymphadenopathy |
Hemic and Lymphatic Diseases |
| C0520679 |
BXGD009101 |
Sleep Apnea, Obstructive |
Respiratory Tract Diseases; Nervous System Diseases |
| C0521525 |
BXGD009139 |
Short neck |
|
| C0522631 |
BXGD009205 |
Acute myeloid leukemia, minimal differentiation |
Neoplasms |
| C0524620 |
BXGD009236 |
Metabolic Syndrome X |
Nutritional and Metabolic Diseases |
| C0524851 |
BXGD009246 |
Neurodegenerative Disorders |
Nervous System Diseases |
| C0541764 |
BXGD009259 |
Delayed bone age |
|
| C0542476 |
BXGD009276 |
Forgetful |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C0545053 |
BXGD009323 |
Advanced bone age |
|
| C0548883 |
BXGD009356 |
Low frustration tolerance |
Behavior and Behavior Mechanisms |
| C0553580 |
BXGD009399 |
Ewings sarcoma |
Neoplasms |
| C0557874 |
BXGD009444 |
Global developmental delay |
|
| C0566602 |
BXGD009489 |
Primary sclerosing cholangitis |
Digestive System Diseases |
| C0566899 |
BXGD009494 |
Small labia majora |
|
| C0575802 |
BXGD009521 |
Small hand |
|
| C0575897 |
BXGD009524 |
Thumb deformity |
Musculoskeletal Diseases |
| C0576226 |
BXGD009527 |
Short foot |
|
| C0578038 |
BXGD009542 |
Thin lips |
|
| C0585442 |
BXGD009593 |
Osteosarcoma of bone |
Neoplasms |
| C0595989 |
BXGD009632 |
Carcinoma of larynx |
Neoplasms; Respiratory Tract Diseases; Otorhinolaryngologic Diseases |
| C0596263 |
BXGD009639 |
Carcinogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0598766 |
BXGD009669 |
Leukemogenesis |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0598894 |
BXGD009673 |
Monocytic leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C0598935 |
BXGD009674 |
Tumor Initiation |
Pathological Conditions, Signs and Symptoms; Neoplasms |
| C0600104 |
BXGD009690 |
Obsessive compulsive behavior |
Behavior and Behavior Mechanisms |
| C0600139 |
BXGD009695 |
Prostate carcinoma |
Neoplasms; Male Urogenital Diseases |
| C0678222 |
BXGD009749 |
Breast Carcinoma |
Neoplasms; Skin and Connective Tissue Diseases |
| C0678230 |
BXGD009750 |
Congenital Epicanthus |
|
| C0683322 |
BXGD009782 |
Mental impairment |
|
| C0684249 |
BXGD009790 |
Carcinoma of lung |
Neoplasms; Respiratory Tract Diseases |
| C0686619 |
BXGD009835 |
Secondary malignant neoplasm of lymph node |
Pathological Conditions, Signs and Symptoms; 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 |
| C0700201 |
BXGD009880 |
Dyssomnias |
Nervous System Diseases; Mental Disorders |
| C0728895 |
BXGD009919 |
Absent finger |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C0740391 |
BXGD009987 |
Middle Cerebral Artery Occlusion |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Cardiovascular Diseases |
| C0745103 |
BXGD010114 |
Hyperlipoproteinemia Type IIa |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C0751606 |
BXGD010523 |
Adult Acute Lymphocytic Leukemia |
|
| C0795816 |
BXGD010737 |
Chromosome 6, monosomy 6q |
Pathological Conditions, Signs and Symptoms |
| C0796004 |
BXGD010776 |
Kabuki make-up syndrome |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Otorhinolaryngologic Diseases; Hemic and Lymphatic Diseases |
| C0848558 |
BXGD010882 |
Hypospadias |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C0851578 |
BXGD010925 |
Sleep Disorders |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders |
| C0853602 |
BXGD010972 |
Immunodeficiency congenital |
|
| C0855095 |
BXGD011071 |
Small Lymphocytic Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0855146 |
BXGD011077 |
B Lymphoblastic Lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C0856053 |
BXGD011091 |
Leukemia secondary |
|
| C0856823 |
BXGD011117 |
Undifferentiated type acute leukemia |
|
| C0856825 |
BXGD011118 |
Acute GVH disease |
Immune System Diseases |
| C0856863 |
BXGD011122 |
Broad-based gait |
|
| C0862039 |
BXGD011257 |
Precursor B-lymphoblastic lymphoma stage II |
|
| C0920028 |
BXGD011454 |
Leukaemia recurrent |
Neoplasms |
| C0948976 |
BXGD011566 |
Leukemic infiltration of skin |
Neoplasms; Skin and Connective Tissue Diseases |
| C1135161 |
BXGD011690 |
Stage 4S neuroblastoma |
|
| C1260959 |
BXGD011846 |
Drusen |
|
| C1261473 |
BXGD011855 |
Sarcoma |
Neoplasms |
| C1263846 |
BXGD011897 |
Attention deficit hyperactivity disorder |
Mental Disorders |
| C1269683 |
BXGD012001 |
Major Depressive Disorder |
Mental Disorders |
| C1269700 |
BXGD012002 |
Caliectasis |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1269955 |
BXGD012005 |
Tumor Cell Invasion |
|
| C1292754 |
BXGD012227 |
Mediastinal (Thymic) Large B-Cell Lymphoma |
Neoplasms; Respiratory Tract Diseases; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1292769 |
BXGD012230 |
Precursor B-cell lymphoblastic leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1292775 |
BXGD012234 |
Acute myeloid leukemia, 11q23 abnormalities |
Neoplasms |
| C1292776 |
BXGD012235 |
Therapy-related acute myeloid leukemia and myelodysplastic syndrome |
Neoplasms |
| C1292778 |
BXGD012237 |
Chronic myeloproliferative disorder |
Neoplasms; Hemic and Lymphatic Diseases |
| C1292780 |
BXGD012239 |
Therapy-related myelodysplastic syndrome |
Hemic and Lymphatic Diseases |
| C1297882 |
BXGD012244 |
Partial Trisomy |
Pathological Conditions, Signs and Symptoms |
| C1301359 |
BXGD012289 |
Precursor T cell lymphoblastic leukemia/lymphoblastic lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C1301363 |
BXGD012292 |
Blastic plasmacytoid dendritic cell neoplasm |
Neoplasms; Skin and Connective Tissue Diseases |
| C1301937 |
BXGD012300 |
Talipes |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C1305855 |
BXGD012348 |
Body mass index |
|
| C1306459 |
BXGD012361 |
Primary malignant neoplasm |
Neoplasms |
| C1306460 |
BXGD012362 |
Primary malignant neoplasm of lung |
Neoplasms; Respiratory Tract Diseases |
| C1306710 |
BXGD012372 |
Facial asymmetry |
Pathological Conditions, Signs and Symptoms |
| C1306759 |
BXGD012374 |
Eosinophilic disorder |
Hemic and Lymphatic Diseases |
| C1318544 |
BXGD012401 |
M5b Acute differentiated monocytic leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C1328407 |
BXGD012465 |
Hip Dysplasia |
Musculoskeletal Diseases; Wounds and Injuries |
| C1328504 |
BXGD012469 |
Hormone refractory prostate cancer |
Neoplasms; Male Urogenital Diseases |
| C1332153 |
BXGD012490 |
acute myeloid leukemia with multilineage dysplasia following myelodysplastic syndrome |
|
| 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 |
| C1332884 |
BXGD012549 |
Central nervous system leukaemia |
Neoplasms |
| C1332965 |
BXGD012565 |
Congenital Mesoblastic Nephroma |
Neoplasms; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1332977 |
BXGD012569 |
Childhood Leukemia |
Neoplasms |
| 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 |
| C1336727 |
BXGD012854 |
Testicular Sarcoma |
Neoplasms; Male Urogenital Diseases; Endocrine System Diseases |
| C1336735 |
BXGD012856 |
Treatment related acute myeloid leukaemia |
|
| C1378511 |
BXGD012932 |
Undifferentiated leukemia |
|
| C1386048 |
BXGD012950 |
Intrauterine retardation |
|
| C1458155 |
BXGD013136 |
Mammary Neoplasms |
Neoplasms; Skin and Connective Tissue Diseases |
| C1519680 |
BXGD013244 |
Tumor Immunity |
Pathological Conditions, Signs and Symptoms |
| C1531647 |
BXGD013301 |
Cerebral ventriculomegaly |
Nervous System Diseases |
| C1535926 |
BXGD013322 |
Neurodevelopmental Disorders |
Mental Disorders |
| C1565489 |
BXGD013401 |
Renal Insufficiency |
Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C1608408 |
BXGD013434 |
Malignant transformation |
|
| C1621958 |
BXGD013468 |
Glioblastoma Multiforme |
Neoplasms |
| C1654637 |
BXGD013484 |
androgen independent prostate cancer |
|
| C1708349 |
BXGD013597 |
Hereditary Diffuse Gastric Cancer |
Digestive System Diseases; Neoplasms |
| C1710026 |
BXGD013636 |
Sclerosing Epithelioid Fibrosarcoma |
Neoplasms |
| C1762616 |
BXGD013753 |
Meningioma, benign, no ICD-O subtype |
Neoplasms; Nervous System Diseases |
| C1827524 |
BXGD013773 |
Wide spaced nipples |
|
| C1836195 |
BXGD014094 |
Short toe |
|
| C1836542 |
BXGD014129 |
Depressed nasal bridge |
|
| C1836842 |
BXGD014167 |
Psychomotor deterioration |
Mental Disorders |
| C1837658 |
BXGD014257 |
Gross motor development delay |
Mental Disorders |
| C1840077 |
BXGD014434 |
Anteverted nostril |
|
| C1841972 |
BXGD014484 |
Glucocorticoid Receptor Deficiency |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases |
| C1842366 |
BXGD014512 |
Low anterior hairline |
|
| C1842581 |
BXGD014525 |
Abnormal corpus callosum morphology |
Pathological Conditions, Signs and Symptoms |
| C1843367 |
BXGD014576 |
Poor school performance |
|
| C1843496 |
BXGD014588 |
Bilateral microphthalmos |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Eye Diseases |
| C1844562 |
BXGD014645 |
Medial flaring of the eyebrow |
|
| C1844813 |
BXGD014679 |
Widely spaced teeth |
|
| C1846950 |
BXGD014848 |
Short middle phalanx of finger |
|
| C1847363 |
BXGD014861 |
Aplasia/Hypoplasia of the ribs |
|
| C1848673 |
BXGD014963 |
Hypoplastic feet |
|
| C1849211 |
BXGD015023 |
Generalized hirsutism |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C1849265 |
BXGD015028 |
Overgrowth |
|
| C1849311 |
BXGD015034 |
Short 1st metacarpal |
|
| C1849367 |
BXGD015046 |
Nasal bridge wide |
|
| C1849510 |
BXGD015061 |
Prenatal movement abnormality |
|
| C1850049 |
BXGD015101 |
Clinodactyly of the 5th finger |
|
| C1853241 |
BXGD015321 |
Flat face |
|
| C1853487 |
BXGD015340 |
Thick eyebrow |
|
| C1853738 |
BXGD015357 |
Long eyelashes |
|
| C1854114 |
BXGD015383 |
Short nose |
|
| C1854630 |
BXGD015416 |
Growth Deficiency and Mental Retardation with Facial Dysmorphism |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C1854928 |
BXGD015443 |
Protuberant abdomen |
|
| C1855728 |
BXGD015536 |
Low posterior hairline |
|
| C1855900 |
BXGD015559 |
HYPERTRICHOSIS, CONGENITAL GENERALIZED |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases |
| C1856121 |
BXGD015578 |
Broad eyebrow |
|
| C1857486 |
BXGD015710 |
Low-set, posteriorly rotated ears |
|
| C1857641 |
BXGD015727 |
Severe postnatal growth retardation |
|
| C1858120 |
BXGD015774 |
Generalized hypotonia |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases |
| C1859236 |
BXGD015867 |
Prolonged neonatal jaundice |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C1859717 |
BXGD015924 |
Depressed nasal tip |
|
| C1859778 |
BXGD015931 |
Postnatal growth retardation |
|
| C1862095 |
BXGD016100 |
Bilateral single transverse palmar creases |
|
| C1865014 |
BXGD016282 |
Long philtrum |
|
| C1865017 |
BXGD016283 |
Thin upper lip vermilion |
|
| C1865572 |
BXGD016331 |
Proximal placement of thumb |
|
| C1865916 |
BXGD016355 |
Bilateral ptosis |
Eye Diseases |
| C1866190 |
BXGD016384 |
Atresia of the external auditory canal |
|
| C1866195 |
BXGD016385 |
Downturned corners of mouth |
|
| C1866730 |
BXGD016419 |
Rhizomelia |
|
| C1868571 |
BXGD016508 |
Highly arched eyebrow |
|
| C1879321 |
BXGD016572 |
Acute Myeloid Leukemia (AML-M2) |
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 |
| C1963101 |
BXGD016683 |
Encephalopathy, CTCAE 3.0 |
|
| C1963184 |
BXGD016688 |
Nystagmus, CTCAE 3.0 |
|
| C2239176 |
BXGD016965 |
Liver carcinoma |
Digestive System Diseases; Neoplasms |
| C2242826 |
BXGD017006 |
Myeloblastic leukemia |
|
| C2315100 |
BXGD017021 |
Pediatric failure to thrive |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases; Mental Disorders |
| C2347761 |
BXGD017049 |
Childhood Myelodysplastic Syndrome |
Hemic and Lymphatic Diseases |
| C2673410 |
BXGD017200 |
Small midface |
|
| C2673670 |
BXGD017220 |
Curly eyelashes |
|
| C2674608 |
BXGD017250 |
Feeding difficulties in infancy |
|
| C2675021 |
BXGD017264 |
Narrow palpebral fissure |
|
| C2697636 |
BXGD017430 |
Hyperdiploid B Acute Lymphoblastic Leukemia |
|
| C2745900 |
BXGD017568 |
Promyelocytic leukemia |
|
| C2825139 |
BXGD017770 |
Acute Myeloid Leukemia with Myelodysplasia-Related Changes |
Neoplasms |
| C2825306 |
BXGD017772 |
Treatment related leukaemia |
Neoplasms |
| C2826025 |
BXGD017783 |
Mixed phenotype acute leukemia |
|
| C2826323 |
BXGD017790 |
Refractory Cytopenia of Childhood |
|
| C2861614 |
BXGD017814 |
AML M5b |
|
| C2919142 |
BXGD017867 |
Short Stature, CTCAE |
|
| C2930974 |
BXGD017923 |
Acute erythroleukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C2930975 |
BXGD017924 |
Acute erythroleukemia - M6a subtype |
Neoplasms; Hemic and Lymphatic Diseases |
| C2930976 |
BXGD017925 |
Acute myeloid leukemia FAB-M6 |
Neoplasms; Hemic and Lymphatic Diseases |
| C2930977 |
BXGD017926 |
Acute erythroleukemia - M6b subtype |
Neoplasms; Hemic and Lymphatic Diseases |
| C2939461 |
BXGD018180 |
Myeloid neoplasm |
Neoplasms; Hemic and Lymphatic Diseases |
| C3150077 |
BXGD018291 |
Mild short stature |
|
| C3278923 |
BXGD018748 |
Dilated ventricles (finding) |
|
| C3279222 |
BXGD018751 |
Aplasia/Hypoplasia of the cerebellum |
|
| C3463824 |
BXGD018899 |
MYELODYSPLASTIC SYNDROME |
Hemic and Lymphatic Diseases |
| C3469521 |
BXGD018910 |
FANCONI ANEMIA, COMPLEMENTATION GROUP A (disorder) |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases |
| C3665983 |
BXGD019314 |
Oral aversion |
|
| C3714581 |
BXGD019415 |
Multicystic Dysplastic Kidney |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases |
| C3714756 |
BXGD019429 |
Intellectual Disability |
Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Mental Disorders; Behavior and Behavior Mechanisms |
| C3714796 |
BXGD019434 |
Isolated somatotropin deficiency |
|
| C3807980 |
BXGD019534 |
Apneic episodes in infancy |
Pathological Conditions, Signs and Symptoms; Respiratory Tract Diseases |
| C3826044 |
BXGD019710 |
Lymphoblastic leukemia in children |
|
| C3831784 |
BXGD019755 |
Acute monocytic/monoblastic leukemia |
Neoplasms; Hemic and Lymphatic Diseases |
| C3839868 |
BXGD019788 |
Cytogenetically normal acute myeloid leukemia |
Neoplasms |
| C3887461 |
BXGD019876 |
Head and Neck Carcinoma |
Neoplasms |
| C3887496 |
BXGD019882 |
Oligodactyly |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases |
| C3888194 |
BXGD019955 |
MIXED LINEAGE LEUKEMIA |
|
| C3896960 |
BXGD020042 |
Childhood Pre-B Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C3896961 |
BXGD020043 |
Adult Pre-B Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C3900098 |
BXGD020106 |
Adult Myelodysplastic Syndrome |
Hemic and Lymphatic Diseases |
| C4021386 |
BXGD020621 |
Abnormality of the elbow |
|
| C4023676 |
BXGD021237 |
Increased nuchal translucency |
Pathological Conditions, Signs and Symptoms |
| C4023808 |
BXGD021268 |
Hyperextensibility at elbow |
|
| C4023915 |
BXGD021274 |
Abnormally low-pitched voice |
|
| C4025295 |
BXGD021630 |
Elbow hypertrichosis |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C4054085 |
BXGD021975 |
Refractory Childhood Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C4054188 |
BXGD021977 |
Ph-Like Acute Lymphoblastic Leukemia |
|
| C4054726 |
BXGD021987 |
Infant Leukemia |
|
| C4054727 |
BXGD021988 |
Infant Acute Lymphoblastic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C4086165 |
BXGD022126 |
Childhood Neuroblastoma |
Neoplasms |
| C4280757 |
BXGD022399 |
Fast-growing nails |
|
| C4281993 |
BXGD022418 |
Neonatal respiratory distress |
Respiratory Tract Diseases |
| C4288302 |
BXGD022478 |
Refractory Adult Acute Lymphoblastic Leukemia |
|
| C4288891 |
BXGD022486 |
Infant T Acute Lymphoblastic Leukemia |
|
| C4288893 |
BXGD022488 |
Infant Acute Biphenotypic Leukemia |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C4317146 |
BXGD022730 |
Acid reflux |
|
| C4324336 |
BXGD022759 |
Hyperleukocytosis |
|
| C4521042 |
BXGD023055 |
Complete Trisomy 21 Syndrome |
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4521228 |
BXGD023057 |
Refractory Acute Lymphoblastic Leukemia |
|
| C4546640 |
BXGD023298 |
Hypertrichosis cubiti short stature |
Pathological Conditions, Signs and Symptoms; Skin and Connective Tissue Diseases |
| C4551472 |
BXGD023303 |
Hypertrophic obstructive cardiomyopathy |
Cardiovascular Diseases |
| C4551560 |
BXGD023349 |
Truncal obesity |
Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases |
| C4551583 |
BXGD023361 |
Cerebral cortical atrophy |
|
| C4551686 |
BXGD023391 |
Malignant neoplasm of soft tissue |
Neoplasms |
| C4551851 |
BXGD023419 |
Cornelia de Lange Syndrome 1 |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases |
| C4554036 |
BXGD023557 |
Nystagmus, CTCAE 5.0 |
|
| C4704767 |
BXGD023680 |
Myelodysplastic Syndrome Acute Myeloid Leukemia |
Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| C4721414 |
BXGD023738 |
Mantle cell lymphoma |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C4721444 |
BXGD023742 |
Burkitt Leukemia |
Neoplasms; Infections; Immune System Diseases; Hemic and Lymphatic Diseases |
| C4721453 |
BXGD023744 |
Peripheral Nervous System Diseases |
Nervous System Diseases |
| C4721505 |
BXGD023746 |
Sarcoma, Myeloid |
Neoplasms |
| C4721532 |
BXGD023752 |
Lymphoma, Non-Hodgkin, Familial |
Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases |
| C4722306 |
BXGD023798 |
Metastatic Neuroblastoma |
Neoplasms |
| C4732730 |
BXGD023895 |
Blood spots |
|