1361
|
|
|
Coenzyme Q7, hydroxylase |
CAT5, CLK-1, CLK1, COQ10D8, HMNR9 |
|
1362
|
|
|
Coenzyme Q8A |
ADCK3, ARCA2, CABC1, COQ10D4, COQ8, SCAR9 |
Autosomal recessive ataxia, Cerebellar ataxia, Cataract, Cerebellar atrophy, Coenzyme q10 deficiency, Congenital neurologic anomalies, Global developmental delay, Gout, Mitochondrial disease, Nystagmus, Spinocerebellar ataxia |
1363
|
|
|
Coenzyme Q8B |
ADCK4, NPHS9 |
Obstructive pulmonary disease, Crohn disease, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Inflammatory bowel disease, Mitochondrial disease, Kawasaki disease, Nephrotic syndrome, Retinitis pigmentosa, Ulcerative colitis |
1364
|
|
|
Coenzyme Q9 |
C16orf49, COQ10D5 |
|
1365
|
|
|
Corin, serine peptidase |
ATC2, CMH30, CRN, Lrp4, PEE5, TMPRSS10 |
|
1366
|
|
|
Coronin 1A |
CLABP, CLIPINA, HCORO1, IMD8, TACO, p57 |
Ankylosing spondylitis, Atrial fibrillation, Autism, Carcinoma, Obstructive pulmonary disease, Color vision deficiency, Crohn disease, Dental caries, Epidermodysplasia verruciformis, Hodgkin lymphoma, Immunodeficiency, Insomnia, Multiple sclerosis, Ocular sarcoidosis, Osteoarthritis, Psoriasis, Rheumatoid arthritis, Sclerosing cholangitis, Severe combined immunodeficiency, Ulcerative colitisView all (5 more) |
1367
|
|
|
Coronin 1B |
CORONIN-2 |
|
1368
|
|
|
Coronin 1C |
HCRNN4 |
|
1369
|
|
|
Coronin 2A |
CLIPINB, IR10, WDR2 |
|
1370
|
|
|
Coronin 2B |
CLIPINC |
|