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CTGA Database Listing
Arab Genomic Studies
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  • Bifid Nose, Renal Agenesis, and Anorectal Malformations
    OMIM # 608980
  • Myasthenic Syndrome, Congenital, 4C, Associated with Acetylcholine Receptor Deficiency
    OMIM # 608931
    CMS4C, Myasthenic Syndrome, Congenital, Type Id, CMS1D, Formerly, CMS ID, Formerly, Myasthenia, Familial Infantile, 1, Formerly, FIM1, Formerly,
  • Choanal Atresia, Posterior
    OMIM # 608911
    PCA,
  • Drug Metabolism, Poor, CYP2D6-Related
    OMIM # 608902
    Drug Metabolism, Ultrarapid, CYP2D6-Related, Debrisoquine, Poor Metabolism of, Debrisoquine, Ultrarapid Metabolism of, Sparteine, Poor Metabolism of, Nortriptyline, Poor Metabolism of, Codeine, Ultrarapid Metabolism of,
  • 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
  • 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
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