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CTGA Database Listing
Arab Genomic Studies
Records found: 2557 Sort by:
  • 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
  • Protein S
    OMIM # 176880
    PROS1, Protein S, Alpha, PSA, Protein S Pseudogene , PROSP, Protein S, Beta , PROS2, PSB
  • Thrombophilia, Hereditary due to Protein C Deficiency, Autosomal Dominant
    OMIM # 176860
    THPH3, Protein C Deficiency, Autosomal dominant, PROC Deficiency, Autosomal dominant, Protein C Deficiency, Acquired
  • Prostate Cancer
    OMIM # 176807
  • Hutchinson-Gilford Progeria Syndrome
    OMIM # 176670
    HGPS, Progeria, Myopathy, Early-Onset, with Progeroid Features,
  • Currarino Syndrome
    OMIM # 176450
    Currarino-Triad, Sacral Agenesis Syndrome, Sacral Agenesis, Hereditary, with Presacral Mass, Anterior Meningocele, and/or Teratoma, and Anorectal Malformation, SCRA1
  • Prader-Willi Syndrome
    OMIM # 176270
    PWS, Prader-Labhart-Willi Syndrome, Prader-Willi Syndrome Chromosome Region, PWCR, Willi-Prader Syndrome, Prader-Willi-Like Syndrome Associated with Chromosome 6
  • Porphyria, Acute Intermittent
    OMIM # 176000
    AIP, Porphyria, Swedish Type, Porphobilinogen Deaminase Deficiency, PBGD Deficiency, Uroporphyrinogen Synthase Deficiency, UPS Deficiency, Porphyria, Acute Intermittent, Nonerythroid Variant, Porphyria, Chester Type, PORC
  • Greig Cephalopolysyndactyly Syndrome
    OMIM # 175700
    GCPS, Polysyndactyly with Peculiar Skull Shape
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