391
|
|
|
Aminomethyltransferase |
GCE, GCE2, GCST, GCVT, NKH |
|
392
|
|
|
ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase |
A3GALNT, A3GALT1, GTB, NAGAT |
Allergic rhinitis, Coronary arteriosclerosis, Coronary artery disease, Coronary heart disease, Diabetes mellitus, Diverticular bleeding, Diverticular diseases, Duodenal ulcer, Gastric ulcer, Graves disease, Ischemic stroke, Mood disorder, Myocardial infarction, Nasopharyngeal carcinoma, Ovarian epithelial carcinoma, Pancreatic neoplasm, Pancreatic carcinoma, Pancreatic cancer, Prostatic neoplasms, Prostate cancer, Stomach carcinoma, Stroke, Thrombosis, Vascular diseasesView all (9 more) |
393
|
|
|
Angiogenin |
ALS9, HEL168, RAA1, RNASE4, RNASE5 |
|
394
|
|
|
Adhesion G protein-coupled receptor D1 |
GPR133, PGR25 |
|
395
|
|
|
Angiopoietin 1 |
AGP1, AGPT, AGPT-1, ANG1, HAE5 |
|
396
|
|
|
Actin like 9 |
HSD21, SPGF53 |
|
397
|
|
|
Ankyrin repeat domain 34A |
ANKRD34 |
|
398
|
|
|
Angiopoietin 2 |
AGPT2, ANG2, LMPHM10 |
|
399
|
|
|
Ankyrin 1 |
ANK, SPH1, SPH2, ankyrin-1 |
8p11.2 deletion syndrome, Accessory rib, Anemia, Atrial septal defect, Azoospermia, Blepharophimosis, Bone disease, Breast cancer, Cholelithiasis, Congenital clubfoot, Congenital coloboma of iris, Congenital epicanthus, Congenital hypoplasia of penis, Cryptorchidism, Developmental delay, Diabetes mellitus, Dwarfism, Fibrinogen deficiency, Gout, Hereditary spherocytosis, High palate, Hyperbilirubinemia, Hypofibrinogenemia, Hypogonadotropic hypogonadism, Mental retardation, Microcephaly, Microcornea, Micrognathism, Mitral valve prolapse, Nystagmus, Patent ductus arteriosus, Restrictive cardiomyopathy, Retinal dystrophy, Spherocytosis, ThrombophiliaView all (20 more) |
400
|
|
|
ATPase phospholipid transporting 11C (ATP11C blood group) |
ATPIG, ATPIQ, HACXL |
|