|
351
|
|
|
Rh blood group D antigen |
CD240D, DIIIc, HDFNRH, RH, RH30, RHCED, RHDVA(TT), RHDel, RHPII, RHXIII, Rh4, RhDCw, RhII, RhK562-II, RhPI, SLC42A5 |
|
|
352
|
|
|
Ras homolog, mTORC1 binding |
RHEB2 |
|
|
353
|
|
|
Rhodopsin |
CSNBAD1, OPN2, RP4 |
Anetoderma, Cataract, Cone-rod dystrophy, Congenital hypoplasia of penis, Congenital sensorineural hearing loss, Congenital stationary night blindness, Cystoid macular edema, Diabetes mellitus, Disorder of eye, Exudative retinopathy, Fundus albipunctatus, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Hypoplasia of optic disc, Keratoconus, Lenticonus, Mental retardation, Myopia, Neuropathy, Night blindness, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Optic disk drusen, Retinal detachment, Retinitis pigmentosa, Retinitis punctata albescens, Rod-cone dystrophy, Strabismus, Congenital stationary night blindness, x-linkedView all (18 more) |
|
354
|
|
|
Ras like without CAAX 2 |
RIBA, RIN, ROC2 |
|
|
355
|
|
|
Ras like without CAAX 1 |
NS8, RIBB, RIT, ROC1 |
Abnormal dermatoglyphic pattern, Atrial septal defect, Blood coagulation disorders, Brachydactyly, Camptodactyly of fingers, Cardiofaciocutaneous syndrome, Cardiomyopathy, Congenital epicanthus, Congenital pectus carinatum, Congenital pectus excavatum, Costello syndrome, Crohn disease, Cryptorchidism, Dwarfism, Dysarthria, Dysmorphic features, Eczema, Fetal ascites, Hearing loss, Hemangioma, High palate, Hydrops fetalis, Hyperkeratosis, Hyperkeratosis pilaris, Hypertrophic cardiomyopathy, Hypogonadotropic hypogonadism, Inflammatory bowel disease, Left ventricular hypertrophy, Leopard syndrome, Lung neoplasms, Lung cancer, Lung carcinoma, Cystic hygroma, Macrocephaly, Melanocytic nevus, Micrognathism, Multiple congenital anomalies, Neck webbing, Noonan syndrome, Noonan-like syndrome with loose anagen hair, Nystagmus, Pericardial effusion, Pleural effusion, Proptosis, Ptosis, Pulmonary stenosis, Radioulnar synostosis, Scoliosis, Strabismus, Ventricular septal defectView all (35 more) |
|
356
|
|
|
Retinaldehyde binding protein 1 |
CRALBP |
Alpers syndrome, Anetoderma, Bothnia retinal dystrophy, Cataract, Congenital hypoplasia of penis, Congenital sensorineural hearing loss, Cystoid macular edema, Diabetes mellitus, Disorder of eye, Eye diseases, Fundus albipunctatus, Glaucoma, Hearing loss, Hyperinsulinism, Hypogonadism, Keratoconus, Lenticonus, Age-related macular degeneration, Mental retardation, Newfoundland rod-cone dystrophy, Nyctalopia, Nystagmus, Obesity, Optic atrophy, Retinal dystrophy, Retinitis pigmentosa, Retinitis punctata albescensView all (12 more) |
|
357
|
|
|
Relaxin 2 |
H2, H2-RLX, RLXH2, bA12D24.1.1, bA12D24.1.2 |
|
|
358
|
|
|
RNA component of mitochondrial RNA processing endoribonuclease |
CHH, NME1, RMRPR, RRP2 |
Alopecia, Anauxetic dysplasia, Anemia, Brachycephaly, Brachydactyly, Cardiomyopathy, Cartilage-hair hypoplasia, Congenital epicanthus, Congenital hypoplastic anemia, Congenital neutropenia, Congenital pectus carinatum, Dwarfism, Eosinophilia, Esophageal atresia, Exfoliative dermatitis, Glucose-6-phosphate transport defect, Heart block, Heart septal defects, Hirschsprung disease, Hypodontia, Hypothyroidism, Impaired cognition, Lymphoma, Lymphopenia, Macrotia, Malabsorption syndrome, Mental retardation, Mesomelia, Metaphyseal chondrodysplasia, Metaphyseal dysplasia without hypotrichosis, Micromelia, Myopia, Nephrotic syndrome, Neutropenia, Omenn syndrome, Pyle metaphyseal dysplasia, Rhizomelia, Scoliosis, Severe combined immunodeficiency disease, Skin neoplasms, Spina bifida, Strabismus, Thyroiditis, Tracheal stenosisView all (29 more) |
|
359
|
|
|
Ribonuclease A family member 3 |
ECP, RAF1, RNS3 |
|
|
360
|
|
|
Ribonuclease A family member 4 |
RAB1, RNS4 |
|
