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CTGA Database Listing
Arab Genomic Studies
Records found: 2829 Sort by:
  • Bifid Nose, Renal Agenesis, and Anorectal Malformations
    OMIM # 608980
  • FRAS1-Related Extracellular Matrix Protein 1
    OMIM # 608944
    FREM1, Chromosome 9 Open Reading Frame 154, C9ORF154
  • Glutathione Synthetase Deficiency
    OMIM # 266130
    5-Oxoprolinuria, Pyroglutamic Aciduria
  • Glutathione Synthetase
    OMIM # 601002
    GSS, GSHS
  • Neu-Laxova Syndrome 1
    OMIM # 256520
    Neu-Laxova Syndrome; NLS
  • Phosphoglycerate Dehydrogenase
    OMIM # 606879
    PHGDH, 3-Phosphogylcerate Dehydrogenase, 3PGDH,
  • Laminin, Beta-2
    OMIM # 150325
    LAMB2, Laminin S, LAMS,
  • Al-Gazali Syndrome
    OMIM # 609465
    Multiple Skeletal Abnormalities with Anterior Segment Anomalies of the Eye and Early Lethality, Al-Gazali Al-Talabani Syndrome
  • Beta-1,3-Galactosyltransferase 6
    OMIM # 615291
    B3GALT6, UDP-Gal:Beta-Gal Beta-1,3-Galactosyltransferase, Polypeptide 6, Galactosyltransferase II, GALTII, Beta-3-GALT6
  • Mitochondrial DNA Depletion Syndrome 2 (Myopathic Type)
    OMIM # 609560
    MTDPS2, Mitochondrial DNA Depletion Myopathy, TK2-Related
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