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CTGA Database Listing
Arab Genomic Studies
Records found: 2588 Sort by:
  • Carnitine Palmitoyltransferase II Deficiency, Lethal Neonatal
    OMIM # 608836
    Carnitine Palmitoyltransferase II Deficiency, Neonatal, Carnitine Palmitoyltransferase II Deficiency, Antenatal, CPT II Deficiency, Lethal Neonatal, CPT2 Deficiency, Lethal Neonatal
  • Transposition of the Great Arteries, Dextro-Looped
    OMIM # 608808
    DTGA, D-TGA
  • Leukodystrophy, Hypomyelinating, 2
    OMIM # 608804
    HLD2, Pelizaeus-Merzbacher-Like Disease, 1, PMLD1
  • Congenital Disorder of Glycosylation, Type Il
    OMIM # 608776
    CDG Il, CDG1L, ALG9-CDG,
  • Microcephaly 5, Primary, Autosomal Recessive
    OMIM # 608716
    MCPH5
  • Wegener Granulomatosis
    OMIM # 608710
    WG
  • Neuropathy, Hereditary Sensory and Autonomic, Type V
    OMIM # 608654
    HSAN5, HSAN V, Insensitivity to Pain, Congenital
  • Joubert Syndrome 3
    OMIM # 608629
    JBTS3
  • Lipodystrophy, Congenital Generalized, Type 1
    OMIM # 608594
    CGL1, Berardinelli-Seip Congenital Lipodystrophy, Type 1, BSCL1, Lipodystrophy, Berardinelli-Seip Congenital, Type 1, Brunzell Syndrome, AGPAT2-Related,
  • Major Depressive Disorder
    OMIM # 608516
    MDD, Unipolar Depression, Seasonal Affective Disorder, SAD
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