|
441
|
|
|
Ras responsive element binding protein 1 |
FINB, HNT, LZ321, RREB-1, Zep-1 |
22q11 deletion syndrome, 22q11 partial monosomy syndrome, 22q11.2 deletion syndrome, Acne, Acrocephaly, Anxiety disorder, Arachnodactyly, Arrhinencephaly, Arthritis, Asthma, Asymmetric crying face association, Atrial septal defect, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Bowel incontinence, Cataract, Choanal atresia, Cholelithiasis, Chronic obstructive pulmonary disease, Congenital clubfoot, Congenital epicanthus, Congenital exomphalos, Congenital hypoplasia of thymus, Congenital malrotation of intestine, Conotruncal anomaly face syndrome, Corneal neovascularization, Cryptorchidism, Developmental delay, Diabetes mellitus, Digeorge syndrome, Dwarfism, Dysphasia, Gastroesophageal reflux disease, Glaucoma, Gout, Gouty arthritis, Hearing loss, Hirschsprung disease, Hydrocephalus, Hyperthyroidism, Hyperuricemia, Hypoparathyroidism, Hypospadias, Hypothyroidism, Immunologic deficiency syndromes, Imperforate anus, Kidney failure, Laryngomalacia, Lymphocytic leukemia, Age-related macular degeneration, Major affective disorder, Mental depression, Mental retardation, Microcephaly, Micrognathism, Microphthalmos, Microstomia, Multiple renal cysts, Multiple sclerosis, Myelomeningocele, Obesity, Optic atrophy, Oral ulcer, Otitis media, Parkinson disease, Patent ductus arteriosus, Persistent truncus arteriosus, Platybasia, Polycystic kidney disease, Polydactyly of toes, Posterior embryotoxon, Ptosis, Renal hypoplasia, Schizophrenia, Scoliosis, Seborrheic dermatitis, Shprintzen syndrome, Specific learning disorder, Strabismus, Tetralogy of fallot, Tricuspid atresia, Uterine anomalies, Ventricular septal defect, Vesicoureteral reflux, Vulval varicesView all (71 more) |
|
442
|
|
|
Ribonucleotide reductase catalytic subunit M1 |
PEOB6, R1, RIR1, RR1 |
Acrania, Adrenocortical carcinoma, Anencephaly, Craniorachischisis, Diastematomyelia, Liver carcinoma, Lung carcinoma, Lung adenocarcinoma, Neural tube defect, Neurenteric cyst, Primary tethered cord syndrome, Spinal cord myelodysplasia |
|
443
|
|
|
Ribonucleotide reductase regulatory subunit M2 |
C2orf48, R2, RR2, RR2M |
|
|
444
|
|
|
Retinoschisin 1 |
RS, XLRS1 |
|
|
445
|
|
|
Ras suppressor protein 1 |
RSP-1 |
|
|
446
|
|
|
Reticulon 1 |
NSP |
|
|
447
|
|
|
Reticulon 2 |
HMNR11, NSP2, NSPL1, NSPLI, SPG12 |
|
|
448
|
|
|
Retinoid X receptor alpha |
NR2B1, RXR-alpha, RXRalpha |
Amyotrophic lateral sclerosis, Lateral sclerosis, Lesion of sciatic nerve, Liver carcinoma, Malignant mesothelioma, Pancreatic adenocarcinoma, Prostatic neoplasms, Prostate cancer, Sciatic nerve neuralgia-neuritis, Sciatic nerve palsy, Sciatic neuritis, Sciatic neuropathy, Thyroid neoplasm, Thyroid carcinoma, Thyroid gland follicular adenoma, Bladder carcinomaView all (1 more) |
|
449
|
|
|
Retinoid X receptor beta |
DAUDI6, H-2RIIBP, NR2B2, RCoR-1, RXR-beta, RXRbeta |
|
|
450
|
|
|
Retinoid X receptor gamma |
NR2B3, RXR-gamma, RXRC, RXRgamma |
|
