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CTGA Database Listing
Arab Genomic Studies
Records found: 2115 Sort by:
  • Arthrogryposis, Distal, Type 2A
    OMIM # 193700
    DA2A, Freeman-Sheldon Syndrome, FSS, Whistling Face-Windmill Vane Hand Syndrome, Craniocarpotarsal Dystrophy, Craniocarpotarsal Dysplasia
  • Adenosine Deaminase
    OMIM # 608958
    ADA, Adenosine aminohydrolase
  • Dentin Matrix Acidic Phosphoprotein 1 (*)
    OMIM # 600980
    DMP1
  • Neuropathy, Hereditary Sensory and Autonomic, Type V
    OMIM # 608654
    HSAN5, HSAN V, Insensitivity to Pain, Congenital
  • Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy
    OMIM # 607250
    SCAN1
  • Carnitine-Acylcarnitine Translocase Deficiency; CACTD
    OMIM # 212138
    SLC25A20, Carnitine-Acylcarnitine Translocase, CACT, Carnitine-Acylcarnitine Carrier, CAC, Carnitine-Acylcarnitine Translocase Deficiency, CACT Deficiency,
  • 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
  • Psoriasis Susceptibility 1
    OMIM # 177900
  • Transfer RNA, Mitochondrial, Aspartic Acid
    OMIM # 590015
    MTTD, tRNA-asp, Mitochondrial
  • Crystallin, Beta-B1 (*)
    OMIM # 600929
    CRYBB1
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