|
461
|
|
|
SMAD family member 6 |
AOVD2, HsT17432, MADH6, MADH7 |
Acrocephaly, Aneurysm of aortic arch, Aortic aneurysm, Aortic coarctation, Aortic valve calcification, Aortic valve disease, Aortic valve insufficiency, Aortic valve sclerosis, Bicuspid aortic valve, Brachycephaly, Carpal tunnel syndrome, Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Craniosynostosis, Hypertension, Hypoplastic left heart syndrome, Metopic synostosis, Radioulnar synostosis, Scaphocephaly, Synostotic anterior plagiocephaly, Synostotic posterior plagiocephaly, Thoracic aortic aneurysm and aortic dissection, TrigonocephalyView all (10 more) |
|
462
|
|
|
SMAD family member 7 |
CRCS3, MADH7, MADH8 |
|
|
463
|
|
|
SMAD family member 9 |
MADH6, MADH9, PPH2, SMAD8, SMAD8/9, SMAD8A, SMAD8B |
Colonic neoplasms, Colorectal adenoma, Colorectal cancer, Colorectal neoplasms, Hamartomatous polyposis, Heritable pulmonary arterial hypertension, Lung diseases, Pulmonary arterial hypertension, Pulmonary arterial hypertension associated with congenital heart disease, Pulmonary hypertension, Pulmonary hypertension with hereditary hemorrhagic telangiectasia |
|
464
|
|
|
Steroid sulfatase |
ARSC, ARSC1, ASC, ES, SSDD, XLI |
Attention deficit hyperactivity disorder, Autism, Colorectal cancer, Cryptorchidism, Developmental delay, Dwarfism, Dysphasia, Fatty liver, Hyperkeratosis, Hypogonadism, Hypohidrosis, Ichthyosis, Ichthyosis congenita, Ichthyosis, x-linked, Leukemia, Lissencephaly, Mental retardation, Minimal brain dysfunction, Neoplasms, Obesity, Placental steroid sulfatase deficiency, Renal aplasia, Renal insufficiency, Rheumatoid arthritis, Seminoma, Speech disorders, Steroid sulfatase deficiency disease, Syndromic ichthyosis, x-linkedView all (13 more) |
|
465
|
|
|
- |
- |
|
|
466
|
|
|
SUZ12 pseudogene 1 |
SUZ12P |
|
|
467
|
|
|
STX17 divergent transcript |
STX17-AS1 |
|
|
468
|
|
|
STAG3 cohesin complex component like 2 (pseudogene) |
STAG3L1, STAG3L2P, STAG3L3 |
|
|
469
|
|
|
Serpin family C member 1 |
AT3, AT3D, ATIII, ATIII-R2, ATIII-T1, ATIII-T2, THPH7 |
Antithrombin deficiency, Blood coagulation disorders, Cerebral thrombosis, Cerebral thrombus, Coronary syndrome, Disseminated intravascular coagulation, Hepatic vein thrombosis, Hereditary thrombophilia, Intracranial thrombosis, Liver failure, Nephrotic syndrome, Portal vein thrombosis, Respiratory distress syndrome, Retinal vein occlusion, Superficial thrombophlebitis, ThrombosisView all (1 more) |
|
470
|
|
|
Septin 2 |
DIFF6, NEDD-5, NEDD5, Pnutl3, SEPT2, Septin-2, hNedd5 |
|
