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CTGA Database Listing
Arab Genomic Studies
Records found: 2870 Sort by:
  • Lymphoma, Non-Hodgkin, Familial
    OMIM # 605027
    Non-Hodgkin Lymphoma, NHL
  • Abdominal Obesity-Metabolic Syndrome
    OMIM # 605552
    AOMS1, Metabolic Syndrome X, Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 1, Metabolic Syndrome, Protection Against
  • Deafness, Autosomal Recessive 27
    OMIM # 605818
    DFNB27
  • Glycine Decarboxylase
    OMIM # 238300
    GLDC, Glycine Cleavage System P Protein, GCSP, Glycine Dehydrogenase,
  • Glycine Encephalopathy
    OMIM # 605899
    GCE, Hyperglycinemia, Nonketotic, NKH, Hyperglycinemia, Transient Neonatal, TNH,
  • Tyrosinemia, Type I
    OMIM # 276700
    Hepatorenal Tyrosinemia, Fumarylacetoacetase Deficiency, FAH Deficiency, Fumarylacetoacetate Hydrolase, FAH, Fumarylacetoacetase
  • Fumarylacetoacetate Hydrolase
    OMIM # 613871
    FAH, Fumarylacetoacetase
  • Zinc Metalloproteinase STE24
    OMIM # 606480
    ZMPSTE24, STE24, S. cerevisiae, Homolog of, FACE1,
  • Solute Carrier Family 26, Member 4
    OMIM # 605646
    SLC26A4, Pendrin, PDS Gene,
  • Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct
    OMIM # 600791
    EVA, Deafness, Autosomal Recessive 4, DFNB4, Neurosensory Nonsyndromic Recessive Deafness 4, NSRD4, Dilated Vestibular Aqueduct, DVA
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