|
851
|
|
|
Cryptic, EGF-CFC family member 1 |
CFC1B, CRYPTIC, DTGA2, HTX2 |
Biliary atresia with splenic malformation syndrome, Congenital malrotation of intestine, Dextro-looped transposition of the great arteries, Double outlet right ventricle, Heterotaxy, visceral, Isolated congenitally uncorrected transposition of the great arteries, Left atrial isomerism, Mesocardia, Polysplenia, Situs ambiguus, Situs inversus, Taussig-bing anomaly, Transposition of great vessels |
|
852
|
|
|
Cytotoxic and regulatory T cell molecule |
CD355 |
|
|
853
|
|
|
Catenin beta like 1 |
C20orf33, IMD99, NAP, P14L, PP8304, dJ633O20.1 |
|
|
854
|
|
|
C-C motif chemokine ligand 28 |
CCK1, MEC, SCYA28 |
|
|
855
|
|
|
Cytochrome P450 family 26 subfamily B member 1 |
CYP26A2, P450RAI-2, P450RAI2, RHFCA |
Arachnodactyly, Brachycephaly, Craniosynostosis, Esophagus neoplasm, Lethal occipital encephalocele-skeletal dysplasia syndrome, Mouth diseases, Obesity, Occipital encephalocele, Oligodactyly, Radiohumeral fusions with other skeletal and craniofacial anomalies, Ramer ladda syndrome, Schizophrenia |
|
856
|
|
|
Cilia and flagella associated protein 298 |
C21orf48, C21orf59, CILD26, DNAAF16, FBB18, Kur |
Asthenozoospermia, Asthma, Bronchiectasis, Ciliary dyskinesia, Asplenia, Congenital pectus excavatum, Corneal dystrophy, Bronchitis, Hearing loss, Hydrocephalus, Kartagener syndrome, Lung diseases, Nasal polyposis, Otitis media, Rhinitis, Scoliosis, Sinusitis, Situs inversusView all (3 more) |
|
857
|
|
|
CUGBP Elav-like family member 4 |
BRUNOL4, CELF-4 |
|
|
858
|
|
|
Core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1 |
C1GALT, T-synthase |
|
|
859
|
|
|
Carbonic anhydrase 10 |
CA-RPX, CARPX, HUCEP-15 |
|
|
860
|
|
|
C-X9-C motif containing 2 |
2310061C15Rik, C16orf61, DC13 |
|
