|
1061
|
|
|
Centrosomal protein 63 |
SCKL6 |
Agenesis of corpus callosum, Congenital microcephaly, Developmental delay, Developmental dyslexia, Dwarfism, Dysmorphic features, Mental retardation, Microcephaly, Microlissencephaly, Neuronal heterotopia, Pachygyria, Renal aplasia, Seckel syndrome, Vesicoureteral reflux |
|
1062
|
|
|
CDK5 regulatory subunit associated protein 3 |
C53, HSF-27, IC53, LZAP, MST016, OK/SW-cl.114, PP1553 |
|
|
1063
|
|
|
Cubilin |
IFCR, IGS, IGS1, MGA1, gp280 |
Anemia, Bipolar disorder, Breast cancer, Bulimia, Cobalamin deficiency, Colonic neoplasms, Colorectal cancer, Colorectal neoplasms, Dementia, Diabetes, Diabetes mellitus, Esophagus neoplasm, Imerslund-grasbeck syndrome, Melanoma |
|
1064
|
|
|
Coiled-coil domain containing 6 |
D10S170, H4, PTC, PTC1, TPC, TST1 |
|
|
1065
|
|
|
Cytoplasmic polyadenylation element binding protein 4 |
CPE-BP4, hCPEB-4 |
|
|
1066
|
|
|
Centrosomal protein 70 |
BITE |
|
|
1067
|
|
|
Coiled-coil domain containing 68 |
SE57-1 |
|
|
1068
|
|
|
Coenzyme A synthase |
DPCK, NBIA6, NBP, PCH12, PPAT, UKR1, pOV-2 |
Cerebellar hypoplasia, Ciliary dyskinesia, Coasy protein-associated neurodegeneration, Coenzyme a synthase protein associated neurodegeneration, Developmental delay, Developmental regression, Distal amyotrophy, Dysarthria, Hypoplasia of corpus callosum, Impaired cognition, Mental depression, Microcephaly, Micrognathism, Neurodegeneration with brain iron accumulation, Obsessive-compulsive disorder, Parkinson disease, Peripheral axonal neuropathy, Spastic quadriplegiaView all (3 more) |
|
1069
|
|
|
CD276 molecule |
4Ig-B7-H3, B7-H3, B7H3, B7RP-2 |
|
|
1070
|
|
|
Cysteine and glycine rich protein 3 |
CLP, CMD1M, CMH12, CRP3, LMO4, MLP |
Cardiomyopathy, Dilated cardiomyopathy, Endocardial fibroelastosis, Hearing loss, Hypertrophic cardiomyopathy, Impaired myocardial contractility, Lipoatrophy, Lipodystrophy, Lung adenocarcinoma, Myopathy, Palmoplantar keratoderma, Paroxysmal atrial fibrillation, Ventricular tachycardia |
