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CTGA Database Listing
Arab Genomic Studies
Records found: 2572 Sort by:
  • 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,
  • Faciodigitogenital Syndrome, Autosomal Recessive
    OMIM # 227330
    Aarskog-Like Syndrome, Kuwait Type Faciodigitogenital Syndrome, Teebi Naguib Al-Awadi Syndrome,
  • Focal Facial Dermal Dysplasia 3, Setleis Type
    OMIM # 227260
    Setleis Syndrome, Bitemporal Forceps Marks Syndrome, Facial Ectodermal Dysplasia, Focal Facial Dermal Dysplasia, Type II
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