481
|
|
|
C-X3-C motif chemokine receptor 1 |
CCRL1, CMKBRL1, CMKDR1, GPR13, GPRV28, V28 |
|
482
|
|
|
Cytochrome b5 type A |
CYB5, MCB5, METAG |
46, xy disorder of sex development, Adrenal hyperplasia, congenital, Ambiguous genitalia, Cerebellar atrophy, Congenital methemoglobinemia, Cryptorchidism, Dwarfism, Endometrioma, Endometriosis, Enlarged polycystic ovaries, Esotropia, Gynecomastia, Hereditary methemoglobinemia, Hypogonadism, Hypoplasia of vagina, Hypospadias, Mental retardation, Male pseudohermaphroditism, Methemoglobinemia, Methemoglobinemia and ambiguous genitalia, Microcephaly, Obesity, Osteoporosis, Penis agenesis, Physiologic amenorrhea, Respiratory distress syndrome, Spastic quadriplegia, Temporal cortical atrophyView all (13 more) |
483
|
|
|
CREB3 regulatory factor |
C5orf41, LRF |
|
484
|
|
|
Centrosomal protein 120 |
CCDC100, JBTS31, SRTD13 |
Agenesis of corpus callosum, Ambiguous genitalia, Asphyxiating thoracic dystrophy, Atrial septal defect, Brachydactyly, Cerebellar hypoplasia, Cerebellar vermis agenesis, Congenital cerebral hernia, Congenital coloboma of iris, Pulmonary hypoplasia, Congenital omphalocele, Cryptorchidism, Dandy-walker syndrome, Developmental delay, Dextrocardia, Dwarfism, Foot polydactyly, Fundus coloboma, Hirschsprung disease, Hydrocephalus, Hypoplasia of corpus callosum, Impaired cognition, Imperforate anus, Jeune syndrome, Jeune thoracic dystrophy, Joubert syndrome, Joubert syndrome with ocular defect, Kidney disease, Macrocephaly, Macrotia, Majewski syndrome, Mental retardation, Micromelia, Microphthalmos, Multiple myeloma, Neck webbing, Nephronophthisis, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory syndrome, Oral cleft, Osteochondrodysplasia, Patent ductus arteriosus, Polydactyly, Polydactyly of toes, Polymicrogyria, Ptosis, Radial polydactyly, Renal cyst, Renal hypoplasia, Renal insufficiency, Retinal coloboma, Retinal dystrophy, Rhizomelia, Scoliosis, Short rib-polydactyly syndrome, Short-rib thoracic dysplasia with or without polydactyly, Situs inversus, Skeletal dysplasia, Strabismus, Syndactyly of the toes, Postaxial hand polydactyly, Ventricular septal defectView all (48 more) |
485
|
|
|
Cytochrome b561 |
CGCytb, CYB561A1, FRRS2, ORTHYP2 |
|
486
|
|
|
Cytochrome b-245 alpha chain |
CGD4, p22-PHOX |
Atherosclerosis, Granulomatous disease, Chronic obstructive pulmonary disease, Diabetes mellitus, Eczema, Gingivitis, Granulomatosis, Heart diseases, Hypertension, Immunologic deficiency syndromes, Inflammatory abnormality of the eye, Kidney failure, Liver cirrhosis, Liver fibrosis, Lupus erythematosus, Lymphadenitis, Malabsorption syndrome, Mediastinal lymphadenopathy, Osteomyelitis, Otitis media, Renal insufficiency, SinusitisView all (7 more) |
487
|
|
|
Cytochrome b-245 beta chain |
AMCBX2, CGD, CGDX, GP91-1, GP91-PHOX, GP91PHOX, IMD34, NOX2, p91-PHOX |
Brain infarction, Granulomatous disease, Chronic obstructive pulmonary disease, Congestive heart failure, Diabetes mellitus, Eczema, Gingivitis, Granulomatosis, Heart failure, Hypertension, Immunologic deficiency syndromes, Inflammatory abnormality of the eye, Kidney disease, Kidney failure, Lupus erythematosus, Lymphadenitis, Malabsorption syndrome, Mediastinal lymphadenopathy, Myocardial infarction, Osteomyelitis, Otitis media, Zellweger syndrome, SinusitisView all (8 more) |
488
|
|
|
Cytochrome c1 |
MC3DN6, UQCR4 |
|
489
|
|
|
CYLD lysine 63 deubiquitinase |
BRSS, CDMT, CYLD1, CYLDI, EAC, FTDALS8, MFT, MFT1, SBS, TEM, USPL2 |
Brooke-spiegler syndrome, Carcinoma, Uterine cervix neoplasm, Cervical cancer, Crohn disease, Cylindromatosis, Head and neck carcinoma, Head and neck neoplasms, Liver carcinoma, Lung carcinoma, Head and neck cancer, Multiple trichoepithelioma, Neoplasms, Skin neoplasms, Thymoma, Thymic carcinomaView all (1 more) |
490
|
|
|
CNKSR family member 3 |
CNK3, CNK3/IPCEF1, MAGI1 |
|