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1041
|
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Cilia and flagella associated protein 69 |
C7orf63, FAP69, SPGF24 |
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1042
|
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Centrosome and spindle pole associated protein 1 |
CSPP, CSPP-L, JBTS21 |
Absence of septum pellucidum, Accessory nipple, Anencephaly, Brachydactyly, Cataract, Cerebellar hypoplasia, Cerebellar vermis agenesis, Colpocephaly, Asplenia, Congenital cerebral hernia, Congenital coloboma of iris, Congenital epicanthus, Congenital hepatic fibrosis, Congenital meningocele, Cryptorchidism, Cystic liver disease, Dandy-walker syndrome, Developmental delay, Double ureter, Duane retraction syndrome, Fibrosis of pancreas, Foot polydactyly, Frontal bossing, Gastroesophageal reflux disease, Hirschsprung disease, Hydrocephalus, Hypoplasia of corpus callosum, Hypospadias, Joubert syndrome, Joubert syndrome with jeune asphyxiating thoracic dystrophy, Lobar holoprosencephaly, Lung diseases, Male pseudohermaphroditism, Meckel syndrome, Meckel-gruber syndrome, Mental retardation, Microcephaly, Microcornea, Micrognathism, Microphthalmos, Multicystic renal dysplasia, Myopia, Nystagmus, Occipital encephalocele, Oculomotor apraxia, Oculovestibuloauditory syndrome, Optic atrophy, Oral cleft, Pancreatic cyst, Polycystic liver disease, Polydactyly, Polydactyly of toes, Polymicrogyria, Ptosis, Renal dysplasia, Renal insufficiency, Retinal dystrophy, Sclerocornea, Scoliosis, Situs inversus, Strabismus, Syndromic microphthalmia, Talipes, Thoracic hypoplasia, True hermaphroditism, Postaxial hand polydactyly, Urethral atresiaView all (52 more) |
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1043
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Coiled-coil domain containing 134 |
OI22 |
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1044
|
|
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Calcitonin receptor |
CRT, CT-R, CTR, CTR1 |
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1045
|
|
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Cytochrome b reductase 1 |
CYB561A2, DCYTB, FRRS3 |
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1046
|
|
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Coenzyme Q8B |
ADCK4, NPHS9 |
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1047
|
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Cadherin like and PC-esterase domain containing 1 |
C7orf58 |
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1048
|
|
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Caldesmon 1 |
CDM, H-CAD, HCAD, L-CAD, LCAD, NAG22, h-CD |
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1049
|
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Cysteine and serine rich nuclear protein 3 |
FAM130A2, MBU1, PPP1R73, TAIP-2, TAIP2 |
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1050
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CEBPA divergent transcript |
ADINR, CEBPA-AS1 |
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