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CTGA Database Listing
Arab Genomic Studies
Records found: 2423 Sort by:
  • Cardiomyopathy, Familial Hypertrophic
    OMIM # 192600
    CMH, Ventricular Hypertrophy, Hereditary, Asymmetric Septal Hypertrophy, ASH, Hypertrophic Subaortic Stenosis, Idiopathic, Cardiomyopathy, Familial Hypertrophic, 1, CMH1, Cardiomyopathy, Sporadic Hypertrophic, 1,
  • Natriuretic Peptide Precursor A
    OMIM # 108780
    NPPA, Atrial Natriuretic Polypeptides, ANP, Cardionatrin, Atrionatriuretic Factor, Atrial Natriuretic Factor, ANF, Pronatriodilatin, PND, Atriopeptin,
  • Angiotensin I-Converting Enzyme
    OMIM # 106180
    ACE1, Dipeptidyl Carboxypeptidase 1, DCP1, Kininase II, Angiotensin I-Converting Enzyme, Plasma Level of, Angiotensin I-Converting Enzyme, Benign Serum Increase, IgA Nephropathy, Progression to Renal Failure in, Susceptibility to, Angiotensin I-Converting Enzyme, Testicular
  • Dedicator of Cytokinesis 8
    OMIM # 611432
    DOCK8
  • Roundabout, Drosophila, Homolog of, 3
    OMIM # 608630
    ROBO3, RB-Inhibiting Gene 1, RBIG1, RIG1
  • Gaze Palsy, Familial Horizontal, with Progressive Scoliosis
    OMIM # 607313
    HGPPS, Ophthalmoplegia, Progressive External, and Scoliosis
  • Anti-Mullerian Hormone Type II Receptor
    OMIM # 600956
    AMHR2, Anti-Mullerian Hormone Receptor, AMHR, Mullerian Inhibiting Substance Type II Receptor, MISR2,
  • Persistent Mullerian Duct Syndrome, Types I and II
    OMIM # 261550
    PMDS, Pseudohermaphroditism, Male Internal, Hernia Uteri Inguinale, Persistent Oviduct Syndrome, Female Genital Ducts in otherwise Normal Male, Mullerian Derivatives, Persistent,
  • Hyperimmunoglobulin E-Recurrent Infection Syndrome, Autosomal Recessive
    OMIM # 243700
    Hyper-IgE Syndrome, Autosomal Recessive, HIES, Autosomal Recessive
  • Glaucoma 3, Primary Congenital, A
    OMIM # 231300
    GLC3A, Glaucoma, Congenital, GLC3, Buphthalmos
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