Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2588 Sort by:
  • Dermatofibrosarcoma Protuberans
    OMIM # 607907
    DFSP, Giant Cell Fibroblastoma
  • Muscular Dystrophy, Congenital Merosin-Deficient, 1A
    OMIM # 607855
    MDC1A, Muscular Dystrophy, Congenital Merosin-Deficient, Muscular Dystrophy, Congenital, Due to Partial LAMA2 Deficiency
  • Neutropenia, Nonimmune Chronic Idiopathic, of Adults
    OMIM # 607847
    Nonimmune Chronic Idiopathic Neutropenia of Adults, NI-CINA
  • Hypotrichosis-Lymphedema-Telangiectasia Syndrome
    OMIM # 607823
    HLTS
  • Craniolenticulosutural Dysplasia
    OMIM # 607812
    CLSD, Boyadjiev-Jabs Syndrome
  • Bile Acid Synthesis Defect, Congenital, 1
    OMIM # 607765
    CBAS1, 3-Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase Deficiency
  • Leukodystrophy, Dysmyelinating, with Oligodontia
    OMIM # 607694
    Dentoleukoencephalopathy
  • Tubulointerstitial Nephritis with Uveitis
    OMIM # 607665
    TINU, Acute Tubulointerstitial Nephritis, ATIN
  • Niemann-Pick Disease, Type C2
    OMIM # 607625
  • Griscelli Syndrome, Type 2
    OMIM # 607624
    GS2, Griscelli Syndrome with Hemophagocytic Syndrome, Albinism, Partial, with Immunodeficiency, Paid Syndrome,
  1. <<
  2. ...
  3. 7
  4. 8
  5. 9
  6. 10
  7. 11
  8. 12
  9. 13
  10. 14
  11. 15
  12. 16
  13. 17
  14. 18
  15. ...
  16. >>