191
|
|
|
Elastin |
ADCL1, SVAS, WBS, WS |
Androgenetic alopecia, Aortic aneurysm, Aortic stenosis, Atrioventricular septal defect, Cutis laxa, Obstructive airway disease, Obstructive pulmonary disease, Congenital venous anomaly, Accessory skin tag, Congenital stenosis of aortic valve, Dermatitis herpetiformis, Diabetic retinopathy, Digestive system disease, Diverticular disease, Age-related macular degeneration, Benign pemphigus, Thoracic aortic aneurysm and aortic dissection, Giant cell arteritis, Hemorrhoid, Hypertension, Polymyositis, Darier disease, Systemic lupus erythematosus, Myocardial ischemia, Chronic obstructive pulmonary disease, Pulmonary fibrosis, Rheumatic aortic stenosis, Rheumatoid arthritis, Rothmund-thomson syndrome, Ruptured abdominal aortic aneurysm, Ruptured aortic aneurysm, Ruptured thoracic aortic aneurysm, Systemic sclerosis, Tetralogy of fallot, Thoracoabdominal aortic aneurysm, Diabetes mellitus type 2, Varicose veins, Williams syndromeView all (23 more) |
192
|
|
|
Elongin A |
ELOA1, SIII, SIII p110, TCEB3, TCEB3A |
|
193
|
|
|
Elongin C |
SIII, TCEB1 |
|
194
|
|
|
ELOVL fatty acid elongase 1 |
CGI-88, IKSHD, Ssc1 |
|
195
|
|
|
ELOVL fatty acid elongase 2 |
SSC2 |
|
196
|
|
|
ELOVL fatty acid elongase 3 |
CIG-30, CIG30 |
|
197
|
|
|
ELOVL fatty acid elongase 4 |
ADMD, CT118, ISQMR, SCA34, STGD2, STGD3 |
Obstructive pulmonary disease, Congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome, Corneal dystrophy, Elsahy-waters syndrome, Erythrokeratodermia with ataxia, Hereditary corneal dystrophy, Retinitis pigmentosa, Rosacea, Spastic ataxia, Spinocerebellar ataxia, Stargardt disease |
198
|
|
|
ELOVL fatty acid elongase 5 |
HELO1, SCA38, dJ483K16.1 |
|
199
|
|
|
ELOVL fatty acid elongase 6 |
FACE, FAE, LCE, hELO2 |
|
200
|
|
|
ELOVL fatty acid elongase 7 |
- |
|
