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CTGA Database Listing
Arab Genomic Studies
Records found: 2870 Sort by:
  • Neuropathy, Hereditary Sensory and Autonomic, Type V
    OMIM # 608654
    HSAN5, HSAN V, Insensitivity to Pain, Congenital
  • Nerve Growth Factor
    OMIM # 162030
    NGF, Nerve Growth Factor , Beta Subunit, NGFB
  • Abnormal Spindle-Like, Microcephaly-Associated
    OMIM # 605481
    ASPM, ASP, Drosophila, Homolog of, MCPH5 Gene
  • Microcephaly 5, Primary, Autosomal Recessive
    OMIM # 608716
    MCPH5
  • Transposition of the Great Arteries, Dextro-Looped
    OMIM # 608808
    DTGA, D-TGA
  • Choanal Atresia, Posterior
    OMIM # 608911
    PCA,
  • 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
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