|
641
|
|
|
Calcium voltage-gated channel auxiliary subunit gamma 5 |
- |
|
|
642
|
|
|
Calcium voltage-gated channel auxiliary subunit gamma 4 |
- |
|
|
643
|
|
|
Clusterin like 1 |
RA337M |
|
|
644
|
|
|
C3 and PZP like alpha-2-macroglobulin domain containing 8 |
ASGD8, K-CAP, VIP |
Anterior segment dysgenesis, Cataract, Colorectal cancer, Colorectal neoplasms, Congenital anomaly of eye, Ectopia lentis, Ectropion uveae, Glaucoma, Hypoplasia of iris, Iridodonesis, Retinal detachment, Segment dysgenesis |
|
645
|
|
|
Chitinase acidic |
AMCASE, CHIT2, TSA1902 |
|
|
646
|
|
|
Coenzyme Q2, polyprenyltransferase |
CL640, COQ10D1, MSA1, PHB:PPT |
Alport syndrome, Anemia, Anhidrosis, Anxiety disorder, Bilateral convulsive seizures, Camptocormia, Central visual impairment, Cerebellar ataxia, Cerebellar atrophy, Coenzyme q10 deficiency, Developmental regression, Dysarthria, Dysautonomia, Epileptic encephalopathy, Erectile dysfunction, Female anorgasmia, Glomerulonephritis, Glomerulosclerosis, Hearing loss, Hypertrophic cardiomyopathy, Hypoalbuminemia, Hypogonadism, Hypohidrosis, Leigh syndrome with nephrotic syndrome, Orofacial dyskinesia, Liver failure, Mental depression, Mental retardation, Motor delay, Multiple system atrophy, Nephritis, Nephrotic syndrome, Neuromuscular dysphagia, Nystagmus, Olivopontocerebellar atrophies, Orthostatic syncope, Pancytopenia, Parkinson disease, Ptosis, Raynaud phenomenon, Renal cyst, Rod-cone dystrophy, Sleep apnea, Specific learning disorder, Striatonigral degenerationView all (30 more) |
|
647
|
|
|
Contactin 6 |
NB3 |
|
|
648
|
|
|
CECR2 histone acetyl-lysine reader |
- |
|
|
649
|
|
|
C-C motif chemokine receptor 10 |
GPR2 |
|
|
650
|
|
|
Chromosome 10 open reading frame 53 |
- |
|
