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CTGA Database Listing
Arab Genomic Studies
Records found: 2565 Sort by:
  • Adiponectin Receptor 1
    OMIM # 607945
    ADIPOR1, CGI45, Progestin and AdipoQ Receptor Family, Member 1, PAQR1,
  • Retinitis Pigmentosa 12
    OMIM # 600105
    RP12, Retinitis Pigmentosa with or without Paraarteriolar Preservation of Retinal Pigment Epithelium, RP with or without Preserved Paraarteriole Retinal Pigment Epithelium, RP with or without PPRPE,
  • Leber Congenital Amaurosis 8
    OMIM # 613835
    LCA8
  • Pulmonary Hypertension, Primary, 1
    OMIM # 178600
    PPH1, PHT, Pulmonary Hypertension, Primary, Dexfenfluramine-Associated, Pulmonary Hypertension, Primary, Fenfluramine-Associated, Pulmonary Hypertension, Primary, 1, with Hereditary Hemorrhagic Telangiectasia, PPH1 with HHT
  • Pyloric Stenosis, Infantile Hypertrophic 1
    OMIM # 179010
    IHPS1, Pyloric Stenosis, Infantile, Pyloric Stenosis, Infantile Hypertrophic, IHPS
  • Pulmonary Hemosiderosis
    OMIM # 178550
  • Pterygia, Mental Retardation, and Distinctive Craniofacial Features
    OMIM # 177980
    Haspeslagh Syndrome
  • Psoriasis Susceptibility 1
    OMIM # 177900
  • Exfoliation Syndrome
    OMIM # 177650
    XFS, Exfoliation Glaucoma, XFG, Pseudoexfoliation Glaucoma, PEXG, Pseudoexfoliation of the Lens, Pseudoexfoliation Syndrome, PEXS
  • Proteus Syndrome
    OMIM # 176920
    Gigantism, Partial, of Hands and Feet, Nevi, Hemihypertrophy, and Macrocephaly
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