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CTGA Database Listing
Arab Genomic Studies
Records found: 2588 Sort by:
  • Microphthalmia with Limb Anomalies
    OMIM # 206920
    MLA, Anophthalmia with Limb Anomalies, Waardenburg Anophthalmia Syndrome, Anophthalmia-Syndactyly, Ophthalmoacromelic Syndrome, Waardenburg Recessive Anophthalmia Syndrome, Anophthalmia-Waardenburg Syndrome, Anophthalmos-Limb Anomalies Syndrome, Crooked Fingers Syndrome, Syndactyly-Anophthalmos Syndrome
  • Formin-Binding Protein 4
    OMIM # 615265
    FNBP4, FBP30, KIAA1014
  • Premature Ovarian Failure 8
    OMIM # 615723
    POF8, Primary Ovarian Insufficiency, POI
  • Stromal Antigen 3
    OMIM # 608489
    STAG3, Stromalin 3, Cohesin Subunit SA3
  • Deafness, Autosomal Recessive 1A
    OMIM # 220290
    DFNB1A
  • Acyl-CoA Dehydrogenase, Long-Chain, Deficiency of
    OMIM # 201460
    ACADL Deficiency, LCAD Deficiency
  • Vitiligo
    OMIM # 193200
    VTLG, Halo Nevi
  • Thyroid Carcinoma, Papillary
    OMIM # 188550
    Papillary Carcinoma of Thyroid , PACT, PTC, TPC, Familial Nonmedullary Thyroid Cancer, FNMTC, Nonmedullary Thyroid Carcinoma, NMTC,
  • Thyroid Carcinoma, Follicular
    OMIM # 188470
    FTC
  • Nasopharyngeal Carcinoma
    OMIM # 607107
    NPCA, NPC, Nasopharyngeal Cancer
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