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CTGA Database Listing
Arab Genomic Studies
Records found: 2555 Sort by:
  • Galloway-Mowat Syndrome 1
    OMIM # 251300
    Galloway Syndrome, Galloway-Mowat Syndrome, Nephrosis-Neuronal Dysmigration Syndrome, Nephrosis-Microcephaly Syndrome
  • Cytochrome P450, Family 4, Subfamily F, Polypeptide 22
    OMIM # 611495
    CYP4F22, Cytochrome P450, Subfamily IVF, Polypeptide 22,
  • Ichthyosis, Congenital, Autosomal Recessive 5
    OMIM # 604777
    ARCI5, Ichthyosis, Nonlamellar and Nonerythrodermic, Congenital, Autosomal Recessive, NNCI, Ichthyosis Congenita III, Ichthyosis Lamellar, 3, LI3,
  • WD Repeat-Containing Protein 73
    OMIM # 616144
    WDR73, HSPC264,
  • Factor VII Deficiency
    OMIM # 227500
    F7 Deficiency, Hypoproconvertinemia,
  • Coagulation Factor VII
    OMIM # 613878
    F7 , Factor VII
  • Myeloma, Multiple
    OMIM # 254500
    Amyloidosis, Systemic , AL, AL Amyloidosis
  • Thrombocythemia 3
    OMIM # 614521
    THCYT3, Thrombocytosis 3
  • Janus Kinase 2
    OMIM # 147796
    JAK2 , JAK2/ETV6 Fusion Gene
  • Parkinson Disease
    OMIM # 168600
    PD, PARK
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