|
781
|
|
|
Centrosomal protein 83 |
CCDC41, NPHP18, NY-REN-58 |
|
|
782
|
|
|
Coiled-coil-helix-coiled-coil-helix domain containing 2 |
C7orf17, MIX17B, MNRR1, NS2TP, PARK22 |
|
|
783
|
|
|
Cytochrome b5 reductase 4 |
NCB5OR, cb5/cb5R, dJ676J13.1 |
|
|
784
|
|
|
Cereblon |
MRT2, MRT2A |
Absence of septum pellucidum, Anencephaly, Attention deficit hyperactivity disorder, Autism, Central visual impairment, Cerebral atrophy, Cortical dysplasia, Developmental delay, Drachtman weinblatt sitarz syndrome, Dyskinetic syndrome, Dyssomnia, Hypoplasia of corpus callosum, Mental retardation, Mental depression, Microcephaly, Motor delay, Multiple myeloma, Non-syndromic intellectual disability, Polymicrogyria, Retinitis pigmentosa and erythrocytic microcytosis, Salaam seizures, Seizure, Sleep disorders, Stereotyped behaviorView all (9 more) |
|
785
|
|
|
Charged multivesicular body protein 1A |
CHMP1, PCH8, PCOLN3, PRSM1, VPS46-1, VPS46A |
Astigmatism, Cerebellar hypoplasia, Congenital clubfoot, Developmental delay, Dysmorphic features, Esotropia, Hyperopia, Hypoplasia of corpus callosum, Mental retardation, Multiple congenital anomalies, Myopia, Pontoneocerebellar hypoplasia |
|
786
|
|
|
Chemokine like factor |
C32, CKLF1, CKLF2, CKLF3, CKLF4, HSPC224, UCK-1 |
|
|
787
|
|
|
Carboxypeptidase A4 |
CPA3 |
|
|
788
|
|
|
Cysteine rich transmembrane BMP regulator 1 |
CRIM-1, S52 |
|
|
789
|
|
|
Coiled-coil domain containing 174 |
C3orf19, HSPC212, IHPM, IHPMR, ctr1 |
Abducens palsy, Cryptorchidism, Developmental delay, Hypoplasia of corpus callosum, Hypotonia, with psychomotor retardation, Hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome, Myopathy, Hypotonia, Strabismus, Ventricular septal defect |
|
790
|
|
|
C-type lectin domain family 1 member B |
1810061I13Rik, CLEC2, CLEC2B, PRO1384, QDED721 |
|
