Home / CTGA Database Listing
CTGA Database Listing
Arab Genomic Studies
Records found: 2572 Sort by:
  • Prune Belly Syndrome
    OMIM # 100100
    PBS, Abdominal Muscles, Absence of, with Urinary Tract Abnormality and Cryptorchidism, Eagle-Barrett Syndrome, EGBRS
  • Apert Syndrome
    OMIM # 101200
    Acrocephalosyndactyly, Type I , ACS1, ACS I
  • Friedreich Ataxia
    OMIM # 229300
    FA, Friedreich Ataxia 1, FRDA1, Friedreich Ataxia with Retained Reflexes; FARR,
  • Brittle Cornea Syndrome 1
    OMIM # 229200
    BCS1, Fragilitas Oculi with Joint Hyperextensibility, Corneal Fragility, Keratoglobus, Blue Sclerae, Joint Hyperextensibility, Dysgenesis Mesodermalis Corneae Et Sclerae, Ehlers-Danlos Syndrome, Type VIB, EDS6B
  • Myofibromatosis, Infantile, 1
    OMIM # 228550
    IMF1, Myofibromatosis, Juvenile, Fibromatosis, Congenital Generalized, CGF
  • Farber Lipogranulomatosis
    OMIM # 228000
    FRBRL, Farber Disease, Ceramidase Deficiency, Acid Ceramidase Deficiency, AC Deficiency, N-Laurylsphingosine Deacylase Deficiency
  • Fanconi-Bickel Syndrome
    OMIM # 227810
    FBS, Hepatorenal Glycogenosis with Renal Fanconi Syndrome, Hepatic Glycogenosis with Fanconi Nephropathy, Hepatic Glycogenosis with Amino Aciduria and Glucosuria, Fanconi Syndrome with Intestinal Malabsorption and Galactose Intolerance, Pseudo-Phlorizin Diabetes, Glycogenosis, Fanconi Type, Glycogen Storage Disease XI
  • Fanconi Anemia, Complementation Group A
    OMIM # 227650
    FANCA, Fanconi Anemia, FA, Fancomi Anemia, Estren-Dameshek Variant, Estren-Dameshek Variant of Fancomi Anemia, Estren-Dameshek Variant of Fanconi Pancytopenia, Estren-Dameshek Variant of Fanconi Pancytopenia Type 1, FA1
  • Fanconi Anemia, Complementation Group C
    OMIM # 227645
    FANCC, FACC, FAC, Fanconi Pancytopenia, Type 3, FA3
  • Factor X Deficiency
    OMIM # 227600
    Stuart-Prower Factor Deficiency, F10 Deficiency,
  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. >>