Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "R"
371 to 380 of 759 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

371
Rhomboid like 1
RHBDL, RRP
Cerebellar ataxia, Spinocerebellar ataxia

372
Rhomboid like 2
RRP2
Atrial fibrillation, Major depressive disorder, Diabetes mellitus type 2

373
Rhomboid like 3
RHBDL4, VRHO
Schizophrenia, Scoliosis

374
Rh blood group CcEe antigens
CD240CE, RH, RH30A, RHC, RHCe(152N), RHE, RHIXB, RHNA, RHPI, Rh4, RhIVb(J), RhVI, RhVIII, SLC42A4
Hemolytic anemia, Rh deficiency syndrome, Rh-null, amorph type

375
Rh family C glycoprotein
C15orf6, PDRC2, RHGK, SLC42A3
Dental caries

376
Rh blood group D antigen
CD240D, DIIIc, HDFNRH, RH, RH30, RHCED, RHDVA(TT), RHDel, RHPII, RHXIII, Rh4, RhDCw, RhII, RhK562-II, RhPI, SLC42A5
Hemolytic anemia, Alpha-1 antichymotrypsin deficiency, Hemolytic disease of fetus and newborn, Rh deficiency syndrome, Rh isoimmunization, Schizophrenia

377
Ras homolog, mTORC1 binding
RHEB2
Non-small-cell lung carcinoma, Central nervous system cancer, Neurodevelopmental disorder, Focal cortical dysplasia, Glioblastoma, Glioma, Hemimegalencephaly, Intellectual developmental disorder, Non-specific syndromic intellectual disability, Oligodendroglioma

378
RHEB like 1
RHEBL1c
Attention deficit hyperactivity disorder, Bipolar disorder

379
Rhodopsin
CSNBAD1, OPN2, RP4
Retinitis pigmentosa, Blindness, Cataract, Cone dystrophy, Cone-rod dystrophy, Congenital stationary night blindness, Exudative retinopathy, Microcephaly, Neuropathy, congenital hypomyelinating, Night blindness, congenital stationary, Nystagmus, Oguchi disease, Optic atrophy, Retinal degeneration, Retinal detachment
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380
Ras homolog family member A
ARH12, ARHA, EDFAOB, RHO12, RHOH12
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Carcinoma, Congenital hemihypertrophy, Coronary artery disease, Craniofacial abnormalities, Ectodermal dysplasia, Gout, Inflammatory bowel disease, Myocardial infarction, Proteinuria, Stomach neoplasms, Substance abuse, Tooth disease
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