|
571
|
|
|
Cordon-bleu WH2 repeat protein like 1 |
COBLR1 |
|
|
572
|
|
|
Cytoplasmic polyadenylation element binding protein 3 |
- |
|
|
573
|
|
|
Chondroitin sulfate synthase 1 |
CHSY, CSS1, ChSy-1, TPBS |
Brachydactyly, Camptodactyly of fingers, Carpal synostosis, Clinodactyly, Developmental delay, Dwarfism, Hypodontia, Hypoplasia of the maxilla, Mental retardation, Microdontia, Micrognathism, Microstomia, Non-obstructive azoospermia, Oligodontia, Optic atrophy, Plagiocephaly, Sensorineural hearing loss, Specific learning disorder, Syndactyly, Syndactyly of fingers, Synophrys, Tarsal coalition, Temtamy preaxial brachydactyly syndromeView all (8 more) |
|
574
|
|
|
Ciliogenesis associated kinase 1 |
ECO, EJM10, ICK, LCK2, MRK, hICK |
Ambiguous genitalia, Brachydactyly, Cryptorchidism, Endocrine-cerebroosteodysplasia, Febrile seizures, Holoprosencephaly, Hydrocephalus, Hypospadias, Mesomelia, Micrognathism, Micromelia, Mouth abnormalities, Myoclonic epilepsy, Myoclonic seizures, Penis agenesis, Photosensitive tonic-clonic seizures, Polydactyly, Radial polydactyly, Renal carcinoma, Rhizomelia, Short rib-polydactyly syndrome, Status epilepticus, SyndactylyView all (8 more) |
|
575
|
|
|
Connector enhancer of kinase suppressor of Ras 2 |
CNK2, KSR2, MAGUIN, MRXSHG |
Attention deficit hyperactivity disorder, Autism, Cerebral atrophy, Colorectal cancer, Developmental delay, Developmental regression, Diabetes mellitus, Dwarfism, Dyskinetic syndrome, Epileptic encephalopathy, Facial paralysis, Gastroesophageal reflux disease, Neurosensory hearing impairment, Hypodontia, Mental retardation, Macrocephaly, Meckel diverticulum, Mental retardation, x-linked, Microcephaly, Non-specifi epileptic encephalopathy, Non-syndromic intellectual disability, x-linked, Nystagmus, Obesity, Optic atrophy, Ptosis, Seizure, Status epilepticus, Syndactyly of the toesView all (13 more) |
|
576
|
|
|
Calsyntenin 1 |
ALC-ALPHA, CDHR12, CST-1, CSTN1, PIK3CD, XB31alpha, alcalpha1, alcalpha2 |
|
|
577
|
|
|
Centrosomal protein 164 |
NPHP15 |
Cataract, Ciliopathies, Congenital hepatic fibrosis, Developmental delay, Dwarfism, Hypertension, Kidney disease, Nephronophthisis, Polydactyly, Premature menopause, Renal dysplasia and retinal aplasia, Retinal dystrophy, Senior-loken syndrome |
|
578
|
|
|
Caspase recruitment domain family member 8 |
CARDINAL, DACAR, DAKAR, NDPP, NDPP1, TUCAN |
|
|
579
|
|
|
CD93 molecule |
C1QR1, C1qR(P), C1qRP, CDw93, ECSM3, MXRA4, dJ737E23.1 |
|
|
580
|
|
|
Chaperonin containing TCP1 subunit 5 |
CCT-epsilon, CCTE, HEL-S-69, HSNSP, PNAS-102, TCP-1-epsilon |
Atrophy of the spinal cord, Breast cancer, Mammary neoplasms, Breast carcinoma, Distal amyotrophy, Dysautonomia, Foot osteomyelitis, Hereditary sensory neuropathy with spastic paraplegia, Hypocholesterolemia, Lung adenocarcinoma, Marfan syndrome, Peripheral axonal neuropathy, Spastic paraplegia |
