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271
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|
|
Acyl-CoA synthetase long chain family member 4 |
ACS4, FACL4, LACS4, MRX63, MRX68, XLID63 |
Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome, Amme complex, Anxiety disorder, Attention deficit hyperactivity disorder, Autism, Colorectal cancer, Developmental delay, Elliptocytosis, Facial paralysis, Neurosensory hearing impairment, Mental retardation, Liver carcinoma, Lung adenocarcinoma, Macrocephaly, Meckel diverticulum, Melancholia, Mental depression, Mental retardation, x-linked, Myopia, Non-syndromic intellectual disability, x-linked, Obesity, Patent ductus arteriosus, Prostatic neoplasms, Prostate cancer, Renal glomerular disease, Renal insufficiency, Seizure, Strabismus, Syndactyly of the toesView all (14 more) |
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272
|
|
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Aldehyde dehydrogenase 1 family member B1 |
ALDH5, ALDHX |
|
|
273
|
|
|
APC membrane recruitment protein 2 |
FAM123A |
|
|
274
|
|
|
Armadillo repeat containing 3 |
CT81, KU-CT-1, VAC8 |
|
|
275
|
|
|
ATP binding cassette subfamily B member 7 |
ABC7, ASAT, Atm1p, EST140535 |
Anemia, Anemia and spinocerebellar ataxia, Developmental delay, Dysarthria, Nystagmus, Rubral tremor, Scoliosis, Sideroblastic anemia, Sideroblastic anemia and spinocerebellar ataxia, x-linked, Speech disorders, Strabismus |
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276
|
|
|
Aldehyde dehydrogenase 1 family member A3 |
ALDH1A6, ALDH6, MCOP8, RALDH3 |
|
|
277
|
|
|
Atonal bHLH transcription factor 7 |
Math5, NCRNA, PHPVAR, RNANC, bHLHa13 |
Cataract, Congenital cataract microcornea with corneal opacity, Esotropia, Glaucoma, congenital, Leukocoria, Microcornea, Microphthalmos, Pendular nystagmus, Persistent fetal vasculature, Persistent hyperplastic primary vitreous, Persistent pupillary membranes, Phthisis bulbi, Retinal nonattachment, Segment dysgenesis, Synechiae |
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278
|
|
|
Aldehyde dehydrogenase 3 family member B1 |
ALDH4, ALDH7 |
|
|
279
|
|
|
ARF like GTPase 5B |
ARL8 |
|
|
280
|
|
|
Adenylate kinase 9 |
AK 9, AKD1, AKD2, C6orf199, C6orf224, SPGF89, dJ70A9.1 |
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