221
|
|
|
EPH receptor A10 |
DFNA88 |
|
222
|
|
|
EGF domain specific O-linked N-acetylglucosamine transferase |
AER61, AOS4, C3orf64, EOGT1 |
Acquired porencephaly, Adams-oliver syndrome, Alopecia, Aplasia cutis congenita, Brachydactyly, Cataract, Cirrhosis, Congenital arteriovenous malformation, Congenital atresia of pulmonary artery, Congenital cerebral hernia, Congenital hepatic fibrosis, Cutis marmorata, Esophageal varix, Hydrocephalus, Leukopenia, Mental retardation, Microphthalmos, Periventricular leukomalacia, Porencephalic cyst, Portal hypertension, Pulmonary arterial hypertension, Strabismus, Syndactyly of fingers, Talipes, Tetralogy of fallotView all (10 more) |
223
|
|
|
EPH receptor A6 |
EHK-2, EHK2, EK12, EPA6, HEK12, PRO57066 |
|
224
|
|
|
EPHA1 antisense RNA 1 |
- |
|
225
|
|
|
Eukaryotic elongation factor 2 kinase |
CaMKIII, HSU93850, eEF-2K |
|
226
|
|
|
EGF containing fibulin extracellular matrix protein 2 |
ARCL1B, FBLN4, MBP1, UPH1 |
Aortic aneurysm, Arachnodactyly, Basal cell neoplasm, Bladder diverticulum, Bowel diverticulosis, Carcinoma, Congenital diaphragmatic hernia, Congenital pectus excavatum, Congestive heart failure, Cutis laxa, Diverticulum of renal calyx, Fibromuscular dysplasia, High palate, Hypothyroidism, Ileus, Lethal arteriopathy syndrome, Lung diseases, Micrognathism, Osteoporosis, Proptosis, Prostatic neoplasms, Prostate cancer, Ptosis, Pulmonary stenosis, Thoracic aortic aneurysm and aortic dissection, Vesicoureteral refluxView all (11 more) |
227
|
|
|
Endogenous retrovirus group W member 1, envelope |
ENV, ENVW, ERVWE1, HERV-7q, HERV-W-ENV, HERV7Q, HERVW, HERVWENV |
|
228
|
|
|
EH domain containing 3 |
PAST3 |
|
229
|
|
|
Eukaryotic translation initiation factor 4B pseudogene 8 |
- |
|
230
|
|
|
Epithelial cell transforming 2 like |
ARHGEF32, C6orf91, FBXO49, LFDH, dJ509I19.2, dJ509I19.3, dJ509I19.5 |
|