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CTGA Database Listing
Arab Genomic Studies
Records found: 2749 Sort by:
  • Epidermolysis Bullosa, Junctional, Herlitz Type
    OMIM # 226700
    Epidermolysis Bullosa Junctionalis, Herlitz Type, JEB-Herlitz Type, Epidermolysis Bullosa, Junctional, Herlitz-Pearson Type, Herlitz-Pearson-Type Epidermolysis Bullosa, Epidermolysis Bullosa Letalis
  • Laminin, Alpha-3
    OMIM # 600805
    LAMA3, Laminin A3, Laminin 5, Alpha-3 Subunit, LAM5, Alpha-3 Subunit, Epiligrin, 170-kd Subunit, BM600
  • Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative
    OMIM # 600802
    SCID, T Cell-Negative, B Cell-Positive, NK Cell-Negative
  • Janus Kinase 3
    OMIM # 600173
    JAK3, Janus Kinase, Leukocyte, JAKL, LJAK
  • Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5
    OMIM # 253700
    LGMDR5, Muscular Dystrophy, Limb-Girdle, Type 2C, LGMD2C, Muscular Dystrophy, Duchenne-Like, Duchenne-Like Muscular Dystrophy, Autosomal Recessive, Type 1; DMDA1, DMDA, Adhalin Deficiency, Secondary, Sarcoglycan, Gamma, Deficiency of, Severe Childhood Autosomal Recessive Muscular Dystrophy, North African Type; SCARMD, Maghrebian Myopathy,
  • Sarcoglycan, Gamma
    OMIM # 608896
    SGCG, Dystrophin-Associated Glycoprotein, 35-KD
  • Bardet-Biedl syndrome 6
    OMIM # 605231
    BBS6
  • MKKS Gene
    OMIM # 604896
    MKKS, MKS, BBS6 Gene, BBS6
  • Mucopolysaccharidosis Type IVA
    OMIM # 253000
    Morquio Syndrome A, MPS IVA, MPS4A, Morquio A Disease, Galactosamine-6-Sulfatase Deficiency, GALNS Deficiency
  • Galactosamine-6-Sulfate Sulfatase
    OMIM # 612222
    GALNS, N-Acetylgalactosamine-Sulfate Sulfatase
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