|
1251
|
|
|
CD247 molecule |
CD3-ZETA, CD3H, CD3Q, CD3Z, CD3ZETA, IMD25, T3Z, TCRZ |
Anorexia, Apraxia, Arthritis, Asthma, Autoimmune diseases, Celiac disease, Eczema, Eosinophilia, Exfoliative dermatitis, Hypothyroidism, Immune system diseases, Immunodeficiency, Immunologic deficiency syndromes, Iridocyclitis, Lupus erythematosus, Oligoarticular arthritis, Otitis media, Pauciarticular chronic arthritis, Polyarthritis, Respiratory tract diseases, Rheumatoid arthritis, Rheumatoid factor-negative polyarticular arthritis, Scleroderma, Severe combined immunodeficiency diseaseView all (9 more) |
|
1252
|
|
|
Component of oligomeric golgi complex 7 |
CDG2E |
Cerebellar atrophy, Cerebral atrophy, Congenital disorder of glycosylation, Congenital heart defects, Congenital nonbullous ichthyosiform erythroderma, Congestive heart failure, Developmental delay, Dwarfism, Gastroesophageal reflux disease, Hydronephrosis, Hypertrichosis, Hypertrophic cardiomyopathy, Hypoglycemia, Hypoplasia of corpus callosum, Micrognathism, Microstomia, Neurogenic urinary bladderView all (2 more) |
|
1253
|
|
|
CD4 molecule |
CD4mut, IMD79, Leu-3, OKT4D, T4 |
|
|
1254
|
|
|
Cyclin Q |
CycM, FAM58A |
Aortic valve insufficiency, Bicuspid aortic valve, Camptodactyly of fingers, Congenital hypoplasia of radius, Diabetes mellitus, Duane retraction syndrome, Dwarfism, Ectopic kidney, Heart septal defects, Horseshoe kidney, Hypertrophy of clitoris, Imperforate anus, Age-related macular degeneration, Myopia, Pelvic kidney, Peripheral pulmonary artery stenosis, Renal agenesis, Renal insufficiency, Spina bifida occulta, Syndactyly of the toes, Syndactyly-telecanthus-anogenital and renal malformations syndrome, Syringomyelia, Toe syndactyly, telecanthus, and anogenital and renal malformations, Vesicoureteral refluxView all (9 more) |
|
1255
|
|
|
CTBP1 divergent transcript |
C4orf42, CTBP1-AS1, CTBP1-AS2, DDUP |
|
|
1256
|
|
|
CD5 molecule |
LEU1, T1 |
|
|
1257
|
|
|
CD5 molecule like |
AIM, API6, CT-2, PRO229, SP-ALPHA, Spalpha, hAIM |
|
|
1258
|
|
|
Cadherin related family member 1 |
CORD15, PCDH21, PRCAD, RP65 |
Cataract, Cone-rod dystrophy, Congenital hypoplasia of penis, Diabetes mellitus, Disorder of eye, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Leber congenital amaurosis, Mental retardation, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophyView all (4 more) |
|
1259
|
|
|
CD6 molecule |
TP120 |
|
|
1260
|
|
|
Chromosome 1 open reading frame 105 |
- |
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