|
781
|
|
|
ADAM metallopeptidase with thrombospondin type 1 motif 10 |
ADAM-TS10, ADAMTS-10, WMS, WMS1 |
Aortic valve sclerosis, Brachycephaly, Brachydactyly, Carpal tunnel syndrome, Cataract, Dwarfism, Ectopia lentis, Glaucoma, Hypoplasia of the maxilla, Hypoplasia of thumb, Mental retardation, Microspherophakia, Myopia, Patent ductus arteriosus, Pulmonary stenosis, Scoliosis, Spade-like hand, Thoracic aortic aneurysm and aortic dissection, Ventricular septal defect, Weill-marchesani syndromeView all (5 more) |
|
782
|
|
|
AT-rich interaction domain 1A |
B120, BAF250, BAF250a, BM029, C1orf4, CSS2, ELD, MRD14, OSA1, P270, SMARCF1, hELD, hOSA1 |
Adenocarcinoma, African burkitt`s lymphoma, Aortic coarctation, Atrial septal defect, Urinary bladder cancer, Bladder neoplasm, Brachydactyly, Breast adenocarcinoma, Breast cancer, Breast carcinoma, Burkitt`s lymphoma, Carcinoma, Cataract, Central hypothyroidism, Cerebellar hypoplasia, Cholangiocarcinoma, Coffin-siris syndrome, Colorectal cancer, Colorectal neoplasms, Congenital clubfoot, Congenital diaphragmatic hernia, Congenital epicanthus, Congenital heart defects, Hypoplastic aortic arch, Hypoplastic tricuspid valve, Cryptorchidism, Cutis marmorata, Dandy-walker syndrome, Developmental delay, Double outlet right ventricle, Dwarfism, Ectopic kidney, Embryonal rhabdomyosarcoma, Endometrial neoplasms, Endometrial carcinoma, Esophageal cancer, Gastric cancer, Granulomatous slack skin, High palate, Holoprosencephaly, Hydronephrosis, Hypertrichosis, Hypoplasia of corpus callosum, Hypoplastic left heart syndrome, Intrahepatic cholangiocarcinoma, Liver carcinoma, Lymphoma, Macroglossia, Macrostomia, Malignant neoplasm, Mental retardation, Microcephaly, Nasopharyngeal carcinoma, Nephroblastoma, Neuroblastoma, Nystagmus, Ovarian carcinoma, Partial agenesis of corpus callosum, Patent ductus arteriosus, Periventricular leukomalacia, Prostatic neoplasms, Prostate cancer, Ptosis, Renal carcinoma, Scoliosis, Sezary syndrome, Spina bifida occulta, Stomach neoplasms, Strabismus, T-cell lymphoma, Ventricular septal defect, Wilms tumorView all (57 more) |
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783
|
|
|
Acyl-CoA oxidase 2 |
BCOX, BRCACOX, BRCOX, CBAS6, THCCox |
|
|
784
|
|
|
Axin 1 |
AXIN, CMDOH, PPP1R49 |
Cardiovascular diseases, Caudal duplication anomaly, Colorectal cancer, Congenital duplication of uterus, Double ureter, Endometrial cancer, Endometrial carcinoma, Hepatoblastoma, Liver carcinoma, Medulloblastoma, Micronodular cirrhosis, Prostate adenocarcinoma |
|
785
|
|
|
Axin 2 |
AXIL, ODCRCS |
Adenomatous polyposis, Benign neoplasm of stomach, Cardiomyopathy, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Hereditary nonpolyposis colorectal cancer, Hypodontia, Hypoplasia of the maxilla, Leiomyosarcoma of uterus, Liver carcinoma, Microdontia, Micrognathism, Myocardial ischemia, Oligodontia, Oligodontia-cancer predisposition syndrome, Oligodontia-colorectal cancer syndrome, Polyp of large intestine, Renal carcinoma, Stomach neoplasms, Stomach carcinoma, Bladder carcinomaView all (7 more) |
|
786
|
|
|
Aph-1B gamma-secretase subunit |
APH-1B, PRO1328, PSFL, TAAV688, aph-1beta |
|
|
787
|
|
|
Rho GTPase activating protein 24 |
FILGAP, RC-GAP72, RCGAP72, p73, p73RhoGAP |
|
|
788
|
|
|
Autophagy related 10 |
APG10, APG10L, pp12616 |
|
|
789
|
|
|
Angiopoietin like 6 |
AGF, ARP5 |
|
|
790
|
|
|
Adhesion G protein-coupled receptor V1 |
FEB4, GPR98, MASS1, USH2B, USH2C, VLGR1, VLGR1b |
Anxiety disorder, Atopic ige-mediated allergic disorder, Autism, Cataract, Cerebral cortical atrophy, Cervix carcinoma, Chronic obstructive pulmonary disease, Ciliopathies, Congenital sensorineural hearing loss, Cortical dysplasia, Developmental regression, Disorder of eye, Dyscognitive seizures, Epilepsy with febrile seizures plus, Febrile seizures, Generalized epilepsy with febrile seizures plus, Hallucinations, Hearing loss, Hemianopsia, Hypotonic seizures, Impaired cognition, Lung carcinoma, Mental depression, Microdontia, Myoclonic seizures, Myopia, Nonsyndromic deafness, Nyctalopia, Nystagmus, Obtundation status, Retinal dystrophy, Rod-cone dystrophy, Schizophrenia, Seizure, Subcortical cerebral atrophy, Usher syndromeView all (21 more) |
