901
|
|
|
Cilia and flagella associated protein 95 |
C9orf135 |
|
902
|
|
|
Cilia and flagella associated protein 96 |
C4orf47 |
|
903
|
|
|
CFAP97 domain containing 1 |
C17orf105 |
|
904
|
|
|
CFAP97 domain containing 2 |
- |
|
905
|
|
|
Cilia and flagella associated protein 99 |
- |
|
906
|
|
|
Complement factor B |
AHUS4, ARMD14, BF, BFD, CFAB, CFBD, FB, FBI12, GBG, H2-Bf, PBF2 |
Sickle cell anemia, Anterior uveitis, Atrophic macular degeneration, Hemolytic uremic syndrome, Autoimmune thyroid disease, Brain injuries, C3 glomerulonephritis, Ulcerative colitis, Colorectal cancer, Complement component deficiency, Coronary artery disease, Crohn disease, Diabetes mellitus type 1, Diabetic retinopathy, Eye disease, Glaucoma, Iga nephropathy, Inflammatory bowel disease, Systemic lupus erythematosus, Macular degeneration, Age-related macular degeneration, Major depressive disorder, Membranous glomerulonephritis, Mesangiocapillary glomerulonephritis, Myasthenia gravis, Psoriasis, Rheumatoid arthritis, Sclerosing cholangitisView all (13 more) |
907
|
|
|
Cryptic, EGF-CFC family member 1 |
CFC1B, CRYPTIC, DTGA2, HTX2 |
|
908
|
|
|
Cryptic, EGF-CFC family member 1B |
- |
|
909
|
|
|
Complement factor D |
ADIPSIN, ADN, DF, PFD |
Asbestosis, Complement component deficiency, Congestive heart failure, Cyclic neutropenia, Endometriosis, Glomerulonephritis, Heart failure, Liver cirrhosis, Severe congenital neutropenia, Ovarian cysts, Pulmonary fibrosis |
910
|
|
|
Craniofacial development protein 1 |
BCNT, BUCENTAUR, CENP-29, CP27, SWC5, Yeti, p97 |
Atherosclerosis, Brain aneurysm, Cardiovascular disease, Carotid atherosclerosis, Obstructive pulmonary disease, Coronary artery disease, Dupuytren contracture, Heart failure, Hypertension, Irritable bowel syndrome, Migraine, Moyamoya disease, Diabetes mellitus type 2 |