|
51
|
|
|
APC regulator of Wnt signaling pathway 2 |
APCL, MRT74 |
Accessory kidney, Breast cancer, Mammary neoplasms, Breast carcinoma, Cardiovascular abnormalities, Colorectal cancer, Colorectal neoplasms, Developmental dysplasia of the hip, Craniosynostosis, Cryptorchidism, Developmental delay, Dolichocephaly, Frontal bossing, Hearing loss, Heart septal defects, High palate, Hypoglycemia, Hypospadias, Inflammatory bowel disease, Macrocephaly, Macrotia, Malocclusion, Marfan syndrome, Mental retardation, Micrognathism, Multiple renal cysts, Nervous system neoplasms, Obesity, Patent ductus arteriosus, Precocious puberty, Sacrococcygeal teratoma, Scoliosis, Sotos` syndrome, Strabismus, Urogenital abnormalities, Vesicoureteral refluxView all (21 more) |
|
52
|
|
|
Adenosine deaminase RNA specific |
ADAR1, AGS6, DRADA, DSH, DSRAD, G1P1, IFI-4, IFI4, K88DSRBP, P136 |
Acquired porencephaly, Aicardi goutieres syndrome, Aortic aneurysm, Arrhinencephaly, Arthritis, Autoinflammatory disease, Basal ganglia cysts, Brain atrophy, Breast cancer, Mammary neoplasms, Breast carcinoma, Cerebral atrophy, Chilblain lesions, Choreoathetosis, Cutis marmorata, Degeneration of the striatum, Demyelinating neuropathy, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Dysarthria, Dyschromatosis symmetrica hereditaria, Dysphagia, Dystonia, Enchondroma, Gastroesophageal reflux disease, Glaucoma, Glaucoma, congenital, Hemiplegia/hemiparesis, Horizontal pendular nystagmus, Hypertrophic cardiomyopathy, Hypoplasia of corpus callosum, Hypothyroidism, Lymphocytic leukemia, Leukodystrophy, Lipoatrophy, Lipodystrophy, Lung carcinoma, Marfan syndrome, Mental retardation, Microcephaly, Movement disorders, Myositis, Alloimmune thrombocytopenia, Nystagmus, Optic atrophy, Panniculitis, Penis agenesis, Plagiocephaly, Porencephalic cyst, Pseudo-torch syndrome, Ptosis, Raynaud phenomenon, Scoliosis, Spastic quadriplegia, Spastic tetraparesis, Striatal necrosis, Striatonigral degeneration, Symmetrical dyschromatosis of extremitiesView all (45 more) |
|
53
|
|
|
Aldo-keto reductase family 1 member A1 |
ALDR1, ALR, ARM, DD3, HEL-S-6 |
|
|
54
|
|
|
ATP binding cassette subfamily A member 7 |
ABCA-SSN, ABCX, AD9 |
Alzheimer disease, Aphasia, Cerebral cortical atrophy, Dysgraphia, Hallucinations, Language disorders, Mental depression, Mental retardation, Oculomotor apraxia, Oculovestibuloauditory syndrome, Parkinson disease, Semantic dementia, Senile dementia, Senile plaques |
|
55
|
|
|
ATP binding cassette subfamily A member 10 |
EST698739 |
|
|
56
|
|
|
ATP binding cassette subfamily A member 9 |
EST640918 |
|
|
57
|
|
|
ATP binding cassette subfamily A member 8 |
- |
|
|
58
|
|
|
Adenosine deaminase RNA specific B1 |
ADAR2, DRABA2, DRADA2, NEDHYMS, RED1 |
|
|
59
|
|
|
APOA1 antisense RNA |
- |
|
|
60
|
|
|
Acetyl-CoA acyltransferase 2 |
DSAEC, T1 |
|
