|
381
|
|
|
Retinitis pigmentosa GTPase regulator |
COD1, CORDX1, CRD, PCDX, RP15, RP3, XLRP3, orf15 |
Achromatopsia, Asthenozoospermia, Asthma, Bronchiectasis, Bronchitis, Cataract, Ciliary dyskinesia, Ciliopathies, Cone dystrophy, Cone monochromatism, Cone-rod dystrophy, Asplenia, Congenital hypoplasia of penis, Congenital pectus excavatum, Corneal dystrophy, Diabetes mellitus, Disorder of eye, Dyschromatopsia, Exotropia, Glaucoma, Hearing loss, Hydrocephalus, Hyperinsulinism, Hyperopia, Hypogonadism, Kartagener syndrome, Keratoconus, Lung diseases, Age-related macular degeneration, Macular degeneration, x-linked, Macular dystrophy, Mental retardation, Myopia, Nasal polyposis, Night blindness, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Otitis media, Pendular nystagmus, Ciliary dyskinesia-retinitis pigmentosa syndrome, Prostate cancer, Retinal dystrophy, Retinitis pigmentosa, Retinitis pigmentosa, x-linked, Rhinitis, Rod-cone dystrophy, Scoliosis, Sinusitis, Situs inversus, Staphyloma posticumView all (37 more) |
|
382
|
|
|
Retinoid isomerohydrolase RPE65 |
BCO3, LCA2, RP20, mRPE65, p63, rd12, sRPE65 |
Acth deficiency, Amaurosis, Blindness, Cataract, Ciliopathies, Dysgenesis neuroepithelialis retinae, Congenital blindness, Congenital cerebral hernia, Congenital hypoplasia of penis, Developmental delay, Diabetes mellitus, Disorder of eye, Eye diseases, Glaucoma, Hearing loss, Hemiplegia/hemiparesis, Hereditary leber optic atrophy, Hyperinsulinism, Hypogonadism, Keratoconus, Leber congenital amaurosis, Malformation of cortical development, Mental retardation, Motor manifestations, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal diseases, Retinal dystrophy, Retinitis pigmentosa, Rod-cone dystrophyView all (17 more) |
|
383
|
|
|
Ribosomal protein L3 |
ASC-1, L3, TARBP-B, uL3 |
|
|
384
|
|
|
Ribosomal protein L3 like |
CMD2D |
|
|
385
|
|
|
Ribosomal protein L5 |
L5, MSTP030, PPP1R135, uL18 |
Aase-smith syndrome, Anemia, Aplastic anemia, Atrial septal defect, Blackfan-diamond anemia, Aplasia of the ovary, Corpus luteum cyst, Diamond-blackfan anemia, Dwarfism, Erythroid hypoplasia, Hemangioma, Hypoplasia of thumb, Leukemia, Leukopenia, Lymphoblastic leukemia, Macrocephaly, Micrognathism, Microspherocytosis, Migraine, Mitral valve prolapse, Multiple congenital anomalies, Ovarian cysts, Patent ductus arteriosus, Pulmonary arterial hypertension, Testicular hydrocele, Tetralogy of fallot, Tracheomalacia, Ventricular hypertrophy, Ventricular septal defectView all (14 more) |
|
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, Brachydactyly, Branchioma, Clinodactyly, Congenital camptodactyly, Congenital epicanthus, Cryptorchidism, Developmental delay, Dolichocephaly, Dwarfism, Gastroesophageal reflux disease, Hearing loss, Hypospadias, Intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome, x-linked, Laryngomalacia, Lymphoblastic leukemia, Malocclusion, Mental retardation, Microcephaly, Microcephaly-growth retardation-prognathism-cryptorchidism syndrome, x-linked, Microstomia, Myopia, Partington syndrome, Prostatic neoplasms, Prostate cancer, Sacral lipoma, Scoliosis, Spondyloepiphyseal dysplasia, Syndactyly of fingers, Syndromic mental retardation, x-linkedView all (15 more) |
|
389
|
|
|
Ribosomal protein L11 |
DBA7, GIG34, L11, uL5 |
Anemia, Blackfan-diamond anemia, Choanal atresia, Diamond-blackfan anemia, Dwarfism, Eosinophilia, Hypoplasia of thumb, Leukemia, Migraine, Neutropenia, Osteopenia, Osteoporosis, Otitis media, Patent ductus arteriosus, Patent foramen ovale, Prostatic neoplasms, Prostate cancer, Scoliosis, Secundum atrial septal defect, Sprengel deformity, Ventricular septal defectView all (6 more) |
|
390
|
|
|
Ribosomal protein L12 |
L12, uL11 |
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