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CTGA Database Listing
Arab Genomic Studies
Records found: 2749 Sort by:
  • CD27 Antigen
    OMIM # 186711
    CD27, Tumor Necrosis Factor Receptor Superfamily, Member 7, TNFRSF7, T-Cell Activation Antigen S152, S152
  • Lymphoproliferative Syndrome 2
    OMIM # 615122
    LPFS2, CD27 Deficiency,
  • Fructose Intolerance, Hereditary
    OMIM # 229600
    Fructosemia, Fructose-1-Phosphate Aldolase Deficiency, Fructose-1,6-BisphosphateI Aldolase B Deficiency, Aldolase B Deficiency, ALDOB Deficiency
  • Aldolase B, Fructose-Bisphosphate
    OMIM # 612724
    Fructose-1,6-Bisphosphate Aldolase B, Aldolase B, ALDB, Aldolase 2, ALDO2
  • Phosphoserine Aminotransferase 1
    OMIM # 610936
    PSAT1, PSAT, Endometrial Progesterone-Induced Protein, EPIP,
  • Neu-Laxova Syndrome 2
    OMIM # 616038
    NLS2
  • AicardiI-Goutieres Syndrome 2
    OMIM # 610181
    AGS2
  • Ribonuclease H2, Subunit B
    OMIM # 610326
    RNASEH2B, DLEU8, FLJ11712
  • Arylsulfatase A
    OMIM # 607574
    ARSA, Cerebroside-Sulfatase, Cerebroside 3-Sulfatase,
  • Metachromatic Leukodystrophy
    OMIM # 250100
    MLD, Metachromatic Leukoencephalopathy, Cerebral Sclerosis, Diffuse, Metachromatic Form, Sulfatide Lipidosis, Arylsulfatase A Deficiency, ARSA Deficiency, Cerebroside Sulfatase Deficiency, Pseudoarylsulfatase A Deficiency, Metachromatic Leukodystrophy, Late Infantile, Metachromatic Leukodystrophy, Juvenile, Metachromatic Leukodystrophy, Adult
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