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CTGA Database Listing
Arab Genomic Studies
Records found: 2565 Sort by:
  • Cardiomyopathy, Familial Hypertrophic, 1
    OMIM # 192600
    CMH1, CMH, Ventricular Hypertrophy, Hereditary, Asymmetric Septal Hypertrophy, ASH, Hypertrophic Subaortic Stenosis, Idiopathic
  • Long QT Syndrome 1
    OMIM # 192500
    LQT1, Ward-Romano Syndrome, WRS, Romano-Ward Syndrome, RWS, Ventricular Fibrillation with Prolonged QT Interval, Long QT Syndrome 1/2, LQT1/2, Long QT Syndrome 1, Acquired, Susceptibility to
  • VATER Association
    OMIM # 192350
    VACTERL Association
  • ATPase, H+ Transporting, Lysosomal, 56/58-Kd, V1 Subunit B, Isoform 1
    OMIM # 192132
    ATP6V1B1, ATP6B1, Vacuolar Proton Pump, Subunit 3, VPP3,
  • Tuberous Sclerosis 1
    OMIM # 191100
    TSC1, Tuberose Sclerosis, TS, Tuberous Sclerosis Complex, TSC
  • Down Syndrome
    OMIM # 190685
    Trisomy 21, DCR, Down Syndrome Chromosome Region, DSCR, Down Syndrome Critical Region, Transient Myeloproliferative Disorder of Down Syndrome, Leukemia, Megakaryoblastic, of Down Syndrome
  • Trigeminal Neuralgia
    OMIM # 190400
    Tic Douloureux
  • Cutis Laxa, Autosomal Recessive, Type IIIA
    OMIM # 219150
    ARCL3A, De Barsy Syndrome A, Cutis Laxa, Corneal Clouding, and Mental Retardation, Progeroid Syndrome of De Barsy
  • Aldehyde Dehydrogenase 18 Family, Member A1
    OMIM # 138250
    ALDH18A1 , 1-Pyrroline-5-Carboxylate Synthetase , PYCS, P5CS, Glutamate Gamma-Semialdehyde Synthetase , GSAS
  • Inflammatory Skin and Bowel Disease, Neonatal, 1
    OMIM # 614328
    NISBD1
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