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CTGA Database Listing
Arab Genomic Studies
Records found: 2477 Sort by:
  • Abnormal Spindle-Like, Microcephaly-Associated
    OMIM # 605481
    ASPM, ASP, Drosophila, Homolog of, MCPH5 Gene
  • 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,
  • 1-@Acylglycerol-3-Phosphate O-Acyltransferase 2
    OMIM # 603100
    AGPAT2 , Lysophosphatidic Acid Acyltransferase-Beta, LPAAT-Beta,
  • Glucosidase, Beta, Acid (*)
    OMIM # 606463
    GBA, Acid Beta-Glucosidase, Beta-Glucosidase, Acid, Glucocerebrosidase, Glucocerebrosidase Pseudogene, GBAP,
  • Microcephaly 2, Primary, Autosomal Recessive, with or without Cortical Malformations
    OMIM # 604317
    MCPH2
  • WD Repeat-Containing Protein 62
    OMIM # 613583
    WDR62, C19orf14
  • Deafness, Autosomal Recessive 9
    OMIM # 601071
    DFNB9, Neurosensory Nonsyndromic Recessive Deafness 9, NSRD9, Auditory Neuropathy, Autosomal Recessive 1, AUNB1, Auditory Neuropathy, Nonsyndromic Recessive, NSRAN, Auditory Neuropathy, Nonsyndromic Recessive, Temperature-Sensitive
  • Otoferlin
    OMIM # 603681
    OTOF
  • CODAS Syndrome (*)
    OMIM # 600373
    Cerebral, Ocular, Dental, Auricular, and Skeletal Anomalies Syndrome
  • Warburg Micro Syndrome
    OMIM # 600118
    WARBM, Micro Syndrome
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