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CTGA Database Listing
Arab Genomic Studies
Records found: 2378 Sort by:
  • Sulfite Oxidase
    OMIM # 606887
    SUOX
  • Sulfocysteinuria
    OMIM # 272300
    Sulfite Oxidase Deficiency
  • Biotinidase Deficiency
    OMIM # 253260
    Multiple Carboxylase Deficiency, Late-Onset, Multiple Carboxylase Deficiency, Juvenile-Onset, BTD Deficiency
  • Schizophrenia
    OMIM # 181500
    SCZD, Schizoaffective Disorder
  • FYVE, RhoGEF, and PH Domain-Containing Protein 1
    OMIM # 300546
    FGD1
  • Aarskog-Scott Syndrome
    OMIM # 305400
    AAS, Faciogenital Dysplasia, FGDY, Faciodigitogenital Syndrome, Aarskog Syndrome, X-Linked, Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder, Mental Retardation, X-Linked, Syndromic 16, MRXS16,
  • Enhancer of Zeste, Drosophila, Homolog 2
    OMIM # 601573
    EZH2, ENX1
  • Filamin A
    OMIM # 300017
    FLNA, Filamin, Alpha, Filamin 1, FLN1, FLN, Actin-Binding Protein 280, ABP280
  • RHO GTPase-Activating Protein 33
    OMIM # 614902
    ARHGAP33, TC10/CDC42 GTPase-Activating Protein, TCGAP
  • Mitochondrial Poly(A) Polymerase
    OMIM # 613669
    MTPAP
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