|
381
|
|
|
Retinitis pigmentosa GTPase regulator |
COD1, CORDX1, CRD, PCDX, RP15, RP3, XLRP3, orf15 |
Ciliary dyskinesia, Cone dystrophy, Cone dystrophy, x-linked, Cone-rod dystrophy, Cone-rod dystrophy, x-linked, Esophageal atresia, Hearing impairment, Hearing loss, Leber congenital amaurosis, Macular degeneration, Macular dystrophy, Night blindness, congenital stationary, Optic atrophy, Ciliary dyskinesia with retinitis pigmentosa, Respiratory system infectious disease, Retinal degeneration, Retinitis pigmentosa, Retinitis pigmentosa, x-linked, and sinorespiratory infections with or without deafness, Retinitis pigmentosa, x-linked, and sinorespiratory infections, with or without deafness, Retinopathy, X-linked cone-rod dystrophyView all (6 more) |
|
382
|
|
|
Retinoid isomerohydrolase RPE65 |
BCO3, LCA2, RP20, mRPE65, p63, rd12, sRPE65 |
Leber congenital amaurosis , Autism, Retinitis pigmentosa, Blindness, Cone-rod dystrophy, Congenital blindness, Congenital nystagmus, Eye disease, Glaucoma, Global developmental delay, Leber congenital amaurosis, Neurodevelopmental disorders, Nystagmus, Open angle glaucoma, Leber hereditary optic neuropathy, Retinal degeneration, Retinitis pigmentosa with choroidal involvement, Retinopathy, Stargardt diseaseView all (4 more) |
|
383
|
|
|
Ribosomal protein L3 |
ASC-1, L3, TARBP-B, uL3 |
Ankylosing spondylitis, Biliary cirrhosis, Carcinoma, Color vision deficiency, Colorectal cancer, Crohn disease, Macular and posterior pole degeneration, Hypothyroidism, Inflammatory bowel disease, Macular degeneration, Ovarian cancer, Biliary cholangitis, Psoriasis, Retinopathy, Rheumatoid arthritis, Sclerosing cholangitis, Systemic lupus erythematosus, Ulcerative colitisView all (3 more) |
|
384
|
|
|
Ribosomal protein L3 like |
CMD2D |
|
|
385
|
|
|
Ribosomal protein L5 |
L5, MSTP030, PPP1R135, uL18 |
|
|
386
|
|
|
Ribosomal protein L6 |
L6, SHUJUN-2, TAXREB107, TXREB1, eL6 |
|
|
387
|
|
|
Ribosomal protein L9 |
L9, NPC-A-16, uL6 |
|
|
388
|
|
|
Ribosomal protein L10 |
AUTSX5, DXS648, DXS648E, L10, MRXS35, NOV, QM, uL16 |
Autism, Autism, x-linked, Desbuquois syndrome, Intellectual developmental disorder, x-linked, Parkinson disease, Partington syndrome, Prostatic neoplasm, X-linked intellectual disability, X-linked myopathy with excessive autophagy |
|
389
|
|
|
Ribosomal protein L11 |
DBA7, GIG34, L11, uL5 |
|
|
390
|
|
|
Ribosomal protein L12 |
L12, uL11 |
|