|
1051
|
|
|
Calmodulin 1 |
CALML2, CAM2, CAM3, CAMB, CAMC, CAMI, CAMIII, CPVT4, DD132, LQT14, PHKD, PHKD1, caM |
|
|
1052
|
|
|
Coiled-coil domain containing 33 |
CC2D3, CT61, HP11097 |
|
|
1053
|
|
|
Coiled-coil domain containing 170 |
C6orf97, bA282P11.1 |
|
|
1054
|
|
|
Centromere protein T |
C16orf56, CENP-T, SSMGA |
|
|
1055
|
|
|
Cell wall biogenesis 43 C-terminal homolog |
CWH43-C, PGAP2IP |
|
|
1056
|
|
|
CST telomere replication complex component 1 |
AAF-132, AAF132, C17orf68, CRMCC, tmp494178 |
Alopecia, Anemia, Cataract, Cerebroretinal microangiopathy with calcifications and cysts, Cirrhosis, Coats disease, Developmental delay, Diabetes mellitus, Dwarfism, Dysarthria, Dyskeratosis congenita, Epileptic encephalopathy, Esophageal stenosis, Exudative retinopathy, Hypodontia, Hypoplasia of the maxilla, Leukemia, Leukodystrophy, Leukoencephalopathy, Leukoplakia, Liver failure, Lymphoma, Malabsorption syndrome, Metabolic bone disorder, Miller dieker syndrome, Monocytic leukemia, Myelodysplastic syndrome, Nail diseases, Nail dysplasia, Nail dystrophy, Optic atrophy, Osteopenia, Osteoporosis, Palmoplantar keratoderma, Pancreatic neoplasm, Periodontitis, Retinal telangiectasia, Scoliosis, Taurodontism, Tumoral calcinosis, Vascular ectasiaView all (26 more) |
|
1057
|
|
|
Centrosomal protein 290 |
3H11Ag, BBS14, CT87, JBTS5, LCA10, MKS4, NPHP6, POC3, SLSN6, rd16 |
Anencephaly, Arima syndrome, Atrial septal defect, Autism, Bardet-biedl syndrome, Cataract, Cerebellar vermis agenesis, Ciliopathies, Cone-rod dystrophy, Asplenia, Congenital blindness, Congenital cerebral hernia, Congenital coloboma of iris, Congenital hepatic fibrosis, Hypoplasia of the ovary, Congenital hypoplasia of penis, Congenital meningocele, Congenital nystagmus, Cryptorchidism, Cystic liver disease, Dandy-walker syndrome, Developmental delay, Diastrophic dysplasia, Disorder of eye, Double ureter, Drachtman weinblatt sitarz syndrome, Dwarfism, Fibrosis of pancreas, Foot polydactyly, Fundus coloboma, Hemiplegia/hemiparesis, Hirschsprung disease, Hydrocephalus, Hypertension, Hypogonadism, Hypoplasia of corpus callosum, Joubert syndrome, Joubert syndrome with oculorenal defect, Keratoconus, Keratosis follicularis, Kidney disease, Leber congenital amaurosis, Liver fibrosis, Lobar holoprosencephaly, Macular dystrophy, Male pseudohermaphroditism, Malformation of cortical development, Meckel syndrome, Meckel-gruber syndrome, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Mohr-tranebjaerg syndrome, Multicystic renal dysplasia, Nephronophthisis, Nephrotic syndrome, Nystagmus, Obesity, Occipital encephalocele, Oculomotor apraxia, Oculovestibuloauditory syndrome, Optic atrophy, Pancreatic cyst, Polycystic kidney disease, Polycystic liver disease, Polydactyly, Polydactyly of toes, Premature menopause, Ptosis, Renal cyst, Renal dysplasia and retinal aplasia, Renal insufficiency, Retinal coloboma, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophy, Sclerocornea, Scoliosis, Senior-loken syndrome, Situs inversus, Sleep apnea, Speech disorders, Strabismus, Syndactyly of fingers, Syndromic microphthalmia, Talipes, True hermaphroditism, Postaxial hand polydactyly, Urethral atresia, Ventricular septal defectView all (77 more) |
|
1058
|
|
|
Coiled-coil domain containing 92 |
- |
|
|
1059
|
|
|
Cilia and flagella associated protein 43 |
C10orf79, HYDNP1, SPGF19, WDR96, bA373N18.2 |
|
|
1060
|
|
|
Coenzyme Q10B |
- |
|
