Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2501 Sort by:
  • Ectodysplasia A Receptor
    OMIM # 604095
    EDAR, Ectodysplasis 1, Anhidrotic Receptor, Downless, Mouse, Homolog of, DL, Ectodysplasin A1 Isoform Receptor, EDA-A1 Receptor, EDA-A1R, EDA1R,
  • Prune Belly Syndrome
    OMIM # 100100
    PBS, Abdominal Muscles, Absence of, with Urinary Tract Abnormality and Cryptorchidism, Eagle-Barrett Syndrome, EGBRS
  • 5,10-@Methylenetetrahydrofolate Reductase
    OMIM # 607093
    MTHFR
  • Ectodysplasin A
    OMIM # 300451
    EDA, Ectodysplasin, EDA1 Gene, ED1 Gene, ED1, Ectodysplasin A1 Isoform, EDA-A1, Ectodysplasin A2 Isoform, EDA-A2,
  • Ectodermal Dysplasia 1, Hypohidrotic, X-Linked
    OMIM # 305100
    XHED, Ectodermal Dysplasia 1, Hypohidrotic/Hair/Tooth Type, X-Linked, ECTD1, XLHED, Ectodermal Dysplasia, Anhidrotic, X-Linked, EDA, EDA1, Ectodermal Dysplasia, Hypohidrotic, 1, HED1, Ectodermal Dysplasia 1, ED1, Christ-Siemens-Touraine Syndrome, CST Syndrome,
  • Pure Early-Onset Dementia Without Bone Cysts
    OMIM #
  • Triggering Receptor Expressed on Myeloid Cells 2
    OMIM # 605086
    TREM2
  • Dystonia 17, Torsion, Autosomal Recessive
    OMIM # 612406
    DYT17
  • Dyssegmental Dysplasia, Silverman-Handmaker Type
    OMIM # 224410
    DDSH, Silverman-Handmaker Type of Dyssegmental Dysplasia, Dyssegmental Dwarfism, Silverman-Handmaker Type, Anisospondylic Camptomicromelic Dwarfism, Silverman-Handmaker Type
  • Dyssegmental Dysplasia, Rolland-Desbuquois Type
    OMIM # 224400
    Dyssegmental Dysplasia, Anisospondylic Camptomicromelic Dwarfism, Lethal Anisospondylic Camptomicromelic Dwarfism, Rolland-Desbuquois Syndrome, DDRD, Dyssegmental Dwarfism, Rolland-Desbuquois Type, Anisospondylic Camptomicromelic Dwarfism, Rolland-Desbuquois Type
  1. <<
  2. 1
  3. 2
  4. 3
  5. 4
  6. 5
  7. 6
  8. 7
  9. 8
  10. 9
  11. 10
  12. 11
  13. 12
  14. 13
  15. ...
  16. >>