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CTGA Database Listing
Arab Genomic Studies
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  • Familial Hypertriglyceridemia
    OMIM # 145750
    FHTG
  • Malignant Hyperthermia, Susceptibility To, 1
    OMIM # 145600
    MHS1, MHS, Hyperthermia of Anesthesia, Hyperpyrexia, Malignant, MH, King Syndrome, King-Denborough Syndrome, Hyperpyrexia
  • Hypertension, Essential
    OMIM # 145500
    EHT, Primary Hypertension
  • Hypertelorism, Teebi Type
    OMIM # 145420
    Brachycephalofrontonasal Dysplasia, Teebi Syndrome
  • Pseudohypoaldosteronism, Type IIA
    OMIM # 145260
    PHA2A, Hyperpotassemia and Hypertension, Familial, Hypertensive Hyperkalemia, Familial, Gordon Hyperkalemia-Hypertension Syndrome
  • Hyperparathyroidism 1
    OMIM # 145000
    HRPT1, Hyperparathyroidism, Familial Isolated Primary, FIHP, Parathyroid Adenoma, Familial
  • Palmoplantar Keratoderma, Epidermolytic
    OMIM # 144200
    EPPK, Keratoderma, Epidermolytic Palmoplantar, Palmoplantar Keratoderma, Vorner Type, Hyperkeratosis, Localized Epidermolytic, Keratosis Palmaris Et Plantaris Familiaris Tylosis, Keratosis of Greither, Palmoplantar Keratoderma, Epidermolytic, with Knuckle Pads
  • Adrenal Hyperplasia, Congenital, due to 11-Beta-Hydroxylase Deficiency
    OMIM # 202010
    Adrenal Hyperplasia IV, Steroid 11-Beta-Hydroxylase Deficiency, 11-Beta-Hydroxylase Deficiency, Adrenal Hyperplasia, Hypertensive Form, P450C11B1 Deficiency
  • Cytochrome P450, Subfamily XIB, Polypeptide 1
    OMIM # 610613
    CYP11B1, Steroid 11-Beta-Hydroxylase, P450C11
  • Fibroblast Growth Factor Receptor 3
    OMIM # 134934
    FGFR3
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