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CTGA Database Listing
Arab Genomic Studies
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  • Adams-Oliver Syndrome 1
    OMIM # 100300
    AOS1, Absence Defect of Limbs, Scalp, and Skull , AOS, Aplasia Cutis Congenita with Terminal Transverse Limb Defects, Congenital Scalp Defects with Distal Limb Reduction Anomalies
  • Ectodermal Dysplasia 10B, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive
    OMIM # 224900
    ECTD10B, Ectodermal Dysplasia, Hypohidrotic, HED, Ectodermal Dysplasia, Anhidrotic, EDA,
  • 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
  • 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
  • Donohue Syndrome
    OMIM # 246200
    Leprechaunism, Insulin Receptor, Defect in
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