|
221
|
|
|
Aspartylglucosaminidase |
AGU, ASRG, GA |
Acne, Arthritis, Aspartylglucosaminuria, Brachycephaly, Cataract, Cerebral atrophy, Congenital exomphalos, Congenital pectus carinatum, Developmental regression, Dwarfism, Dyskinetic syndrome, Dyssomnia, Fabry disease, Macroglossia, Macrostomia, Malabsorption syndrome, Malocclusion, Mental retardation, Microcephaly, Microtia, Neutropenia, Otitis media, Pfaundler-hurler syndrome, Schizophrenia, Scoliosis, Skin diseases, vascular, Sleep disorders, Speech disorders, Spondylolisthesis, SpondylolysisView all (15 more) |
|
222
|
|
|
Aggrecan |
AGC1, AGCAN, CSPG1, CSPGCP, MSK16, SEDK, SSOAOD |
Arthritis, Brachydactyly, Bronchospasm, Dwarfism, Dysmorphic features, Facioscapulohumeral muscular dystrophy, Frontal bossing, Hypoplasia of thumb, Macrocephaly, Malocclusion, Mesomelia, Micromelia, Multiple congenital anomalies, Osteoarthritis of hip, Osteochondritis dissecans, Rheumatoid arthritis, Rhizomelia, Short stature-advanced bone age osteoarthritis syndrome, Spondyloepimetaphyseal dysplasia, Spondyloepiphyseal dysplasiaView all (5 more) |
|
223
|
|
|
Advanced glycosylation end-product specific receptor |
RAGE, SCARJ1, sRAGE |
Arthritis, Atherosclerosis, Chronic obstructive pulmonary disease, Diabetes mellitus, Diabetic cardiomyopathy, Emphysema, Hyperglycemia, Lewy body disease, Osteoarthrosis deformans, Ovarian epithelial carcinoma, Panacinar emphysema, Pancreatic diseases, Pulmonary emphysema, Rheumatoid arthritis, Schizophrenia, SclerodermaView all (1 more) |
|
224
|
|
|
Amylo-alpha-1,6-glucosidase and 4-alpha-glucanotransferase |
GDE |
Cardiomyopathy, Distal amyotrophy, Dwarfism, Glycogen storage disease, Hyperlipidemia, Hypoglycemia, Immunologic deficiency syndromes, Liver fibrosis, Mental retardation, Myopathy, Ventricular hypertrophy |
|
225
|
|
|
4-aminobutyrate aminotransferase |
GABA-AT, GABAT, NPD009 |
Agenesis of corpus callosum, Autism, Cerebellar hypoplasia, Clonic seizures, Developmental delay, Gamma aminobutyric acid transaminase deficiency, Gastroesophageal reflux disease, Hypotonic seizures, Jacksonian seizure, Leukodystrophy, Malignant neoplasm, Hypotonia, Psychomotor disorders, Seizure |
|
226
|
|
|
Agouti related neuropeptide |
AGRT, ART, ASIP2 |
|
|
227
|
|
|
AT-rich interaction domain 3A |
BRIGHT, DRIL1, DRIL3, E2FBP1 |
|
|
228
|
|
|
Atrophin 1 |
B37, CHEDDA, D12S755E, DRPLA, HRS, NOD |
Action myoclonus-renal failure syndrome, Blepharospasm, Cardiovascular abnormalities, Central visual impairment, Cerebellar ataxia, Cerebral atrophy, Choreoathetosis, Congenital epicanthus, Cryptorchidism, Dementia, Dentatorubral pallidoluysian atrophy, Developmental delay, Dysarthria, Dysphagia, Gastroesophageal reflux disease, Heart septal defects, Hypoplasia of corpus callosum, Inclusion-body disease, May-white syndrome, Mental retardation, Multicystic renal dysplasia, Myoclonic epilepsy, Nuchal bleb, Nystagmus, Otitis media, Polymicrogyria, Posteriorly rotated ear, Scoliosis, Ventricular septal defectView all (14 more) |
|
229
|
|
|
Angiotensinogen |
ANHU, SERPINA8, hFLT1 |
Allanson pantzar mcleod syndrome, Alveolitis, Anemia, Aortic aneurysm, Aortic dissection, Atherosclerosis, Bipolar disorder, Bright disease, Cardiomyopathy, Cardiovascular abnormalities, Cardiovascular diseases, Carotid artery disease, Carotid atherosclerosis, Catalepsy, Cholestasis, Cirrhosis, Clonic seizures, Cognitive disorder, Pulmonary hypoplasia, Congestive heart failure, Coronary artery disease, Diabetic cardiomyopathy, Diabetic nephropathy, Diabetic retinopathy, Essential hypertension, Glomerular hyalinosis, Glomerulonephritis, Glomerulosclerosis, Heart diseases, Heart failure, Hyperemia, Hypertension, Hypotonic seizures, Jacksonian seizure, Kidney disease, Kidney failure, Left ventricular hypertrophy, Liver cirrhosis, Liver fibrosis, Malignant hypertension, Mental depression, Microcephaly, Moyamoya disease, Myocardial diseases, Myocardial infarction, Myocardial ischemia, Nephrosis, Pulmonary fibrosis, Renal hypertension, Renal insufficiency, Renal tubular dysgenesis of genetic origin, Renal tubular dysgenesis with choanal atresia and athelia, Retinopathy, SeizureView all (39 more) |
|
230
|
|
|
Angiotensin II receptor type 1 |
AG2S, AGTR1B, AT1, AT1AR, AT1B, AT1BR, AT1R, AT2R1, ATR1, HAT1R |
Allanson pantzar mcleod syndrome, Aortic aneurysm, Pulmonary hypoplasia, Congestive heart failure, Diabetic retinopathy, Essential hypertension, Heart failure, Hypertension, Kidney disease, Microcephaly, Miscarriage, Myocardial infarction, Narcolepsy, Pancreatic ductal carcinoma, Patent ductus arteriosus, Pituitary adenoma, Pituitary neoplasms, Pituitary carcinoma, Renal tubular dysgenesis of genetic origin, Renal tubular dysgenesis with choanal atresia and atheliaView all (5 more) |
