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CTGA Database Listing
Arab Genomic Studies
Records found: 2115 Sort by:
  • Microphthalmia, Isolated 6
    OMIM # 613517
    MCOP6, Microphthalmia, Posterior Nonsyndromic,
  • Weill-Marchesani-like Syndrome
    OMIM # 613195
  • Coiled-Coil and C2 Domains-Containing Protein 2A
    OMIM # 612013
    CC2D2A, KIAA1345,
  • Bernard-Soulier Syndrome
    OMIM # 231200
    BSS, Bleeding Disorder, Platelet-Type, 1, BDPLT1, Platelet Glycoprotein Ib Deficiency, Glycoprotein Ib, Platelet, Deficiency of, Von Willebrand Factor Receptor Deficiency, Bernard-Soulier Syndrome, Type A1, Bernard-Soulier Syndrome, Type B, Bernard-Soulier Syndrome, Type C,
  • Lissencephaly I
    OMIM # 607432
    LIS1 , Lissencephaly Sequence, Isolated, ILS, Lissencephaly, Classic, Subcortical Laminar Heterotopia, SCLH, Subcortical Band Heterotopia, SBH,
  • Myelofibrosis
    OMIM # 254450
    Myelofibrosis with Myeloid Metaplasia, MMM
  • Kinesin Family Member 21A
    OMIM # 608283
    KIF21A, KIAA1708
  • Chemokine, CXC Motif, Ligand 12
    OMIM # 600835
    CXCL12, Stromal Cell-Derived Factor 1, SDF1, Pre-B Cell Growth-Stimulating Factor, PBSF
  • Leber Congenital Amaurosis 1
    OMIM # 204000
    LCA1, Amaurosis Congenita of Leber I, LCA, Retinal Blindness, Congenital , CRB
  • Glaucoma 3, Primary Congenital, A
    OMIM # 231300
    GLC3A, Glaucoma, Congenital, GLC3, Buphthalmos
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