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231
|
|
|
Angiotensin II receptor type 2 |
AT2, ATGR2, MRX88 |
Attention deficit hyperactivity disorder, Autism, Corpus luteum cyst, Developmental delay, Diabetic cardiomyopathy, Facial paralysis, Gastric cancer, Neurosensory hearing impairment, Hypertension, Mental retardation, Left ventricular hypertrophy, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Non-syndromic intellectual disability, x-linked, Obesity, Ovarian cysts, Seizure, Stomach neoplasms, Syndactyly of the toesView all (5 more) |
|
232
|
|
|
Alanine--glyoxylate aminotransferase |
AGT, AGT1, AGXT1, PH1, SPAT, SPT, Ser-PyrAT, TLH6 |
Anemia, Atherosclerosis, Atrioventricular block, Calcinosis cutis, Cutis marmorata, Gangrene, Hyperoxaluria, Kidney disease, Nephrocalcinosis, Nephrolithiasis, Nephronophthisis, Nervous system diseases, Optic atrophy, Osteosclerosis, Peripheral arterial stenosis, Raynaud phenomenon, Renal insufficiency, Retinal diseases, StrokeView all (4 more) |
|
233
|
|
|
ATP binding cassette subfamily A member 1 |
ABC-1, ABC1, CERP, HDLCQTL13, HDLDT1, HPALP1, TGD |
Allergic rhinitis, Alzheimer disease, Anemia, Apolipoprotein a1 deficiency, Atherosclerosis, Carotid artery stenosis, Cicatricial ectropion, Colorectal cancer, Colorectal neoplasms, Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease, Coronary stenosis, Distal amyotrophy, Ectropion, Exudative macular degeneration, Geographic atrophy, Glucocorticoid deficiency, Gout, Gouty arthritis, Hemiplegia/hemiparesis, Hypercholesterolemia, Hyperlipoproteinemia, Hypoalphalipoproteinemia, Hypocholesterolemia, Kidney failure, Left ventricular hypertrophy, Age-related macular degeneration, Metabolic syndrome, Myocardial infarction, Nail diseases, Nail dysplasia, Nail dystrophy, Nervous system diseases, Peripheral axonal neuropathy, Schizophrenia, Syringomyelia, Tangier disease, Alphalipoproteinemia neuropathy, XanthomatosisView all (25 more) |
|
234
|
|
|
Adenosylhomocysteinase |
SAHH, adoHcyase |
Antithrombin deficiency, Cardiomyopathy, Cerebellar hypoplasia, Developmental delay, Developmental regression, Disorder of amino acid metabolism, Esotropia, Fibrinogen deficiency, Glycine n-methyltransferase deficiency, Hepatic methionine adenosyltransferase deficiency, Hepatolenticular degeneration, Hydrops fetalis, Hypoalbuminemia, Hypofibrinogenemia, Hypoplasia of corpus callosum, Inherited errors of amino acid metabolism, Liver carcinoma, Lung adenocarcinoma, Mental retardation, Microcephaly, Motor delay, Muscular dystrophy, Non-alcoholic fatty liver disease, Respiratory failure, S-adenosylhomocysteine hydrolase deficiency, Sensorimotor neuropathyView all (11 more) |
|
235
|
|
|
Argonaute RISC catalytic component 3 |
EIF2C3 |
|
|
236
|
|
|
Aryl hydrocarbon receptor |
FVH3, RP85, bHLHe76 |
Ankylosing spondylitis, Atherosclerosis, Behcet syndrome, Benign neoplasm, Breast cancer, Mammary neoplasms, Breast carcinoma, Cataract, Cholangitis, Chronobiology disorders, Circadian rhythm disorders, Colitis, Congenital heart defects, Congenital hypoplasia of penis, Congenital nystagmus, Crohn disease, Dermatitis, Diabetes mellitus, Dyslipidemias, Esophagus neoplasm, Gastric cancer, Glaucoma, Hearing loss, Hyperinsulinism, Hypertension, Hypogonadism, Keratoconus, Left ventricular hypertrophy, Liver neoplasms, Liver cancer, Liver cirrhosis, Liver fibrosis, Lung adenocarcinoma, Lung carcinoma, Malignant melanoma of skin, Malignant neoplasm, Malignant neoplasm of ureter, Marfan syndrome, Melanoma, Mental retardation, Metabolic diseases, Miscarriage, Neoplasms, Non-alcoholic fatty liver disease, Nystagmus, Obesity, Optic atrophy, Pancreatic neoplasm, Pancreatic cancer, Prostatic neoplasms, Prostate cancer, Psoriasis, Retinitis pigmentosa, Rheumatoid arthritis, Rod-cone dystrophy, Skin carcinoma, Splenic diseases, Stomach neoplasms, Ulcerative colitis, Urinary bladder calculi, Ureteral neoplasms, Vascular diseasesView all (47 more) |
|
237
|
|
|
Anoctamin 6 |
BDPLT7, SCTS, TMEM16F |
|
|
238
|
|
|
AT-rich interaction domain 2 |
BAF200, CSS6, SMARCF3, ZIPZAP, p200 |
Adenocarcinoma, Anterior pituitary dysgenesis, Anxiety disorder, Arachnoid cyst, Attention deficit hyperactivity disorder, Blepharophimosis, Brachydactyly, Cataract, Clinodactyly, Coffin-siris syndrome, Congenital diaphragmatic hernia, Congenital epicanthus, Cryptorchidism, Cutis marmorata, Dandy-walker syndrome, Developmental delay, Dwarfism, Dysmorphic features, Ectopic kidney, Frontal bossing, Gastroesophageal reflux disease, Tourette syndrome, Hydronephrosis, Hypoplasia of corpus callosum, Liver carcinoma, Macrostomia, Mental retardation, Microcephaly, Micrognathism, Motor delay, Nystagmus, Partial agenesis of corpus callosum, Periventricular leukomalacia, Plagiocephaly, Prostatic neoplasms, Prostate cancer, Ptosis, Scoliosis, Spina bifida occulta, Stereotyped behavior, StrabismusView all (26 more) |
|
239
|
|
|
Adenylate cyclase 4 |
AC4 |
|
|
240
|
|
|
Alpha 2-HS glycoprotein |
A2HS, AHS, APMR1, FETUA, HSGA |
Alopecia, Alopecia-mental retardation syndrome, Brachydactyly, Dwarfism, Hypogonadism, Ichthyosis, Mental retardation, Kidney failure, Macrotia, Microcephaly, Nephronophthisis, Perniola krajewska carnevale syndrome, Acute kidney insufficiency, Scoliosis, Tumoral calcinosis |
