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CTGA Database Listing
Arab Genomic Studies
Records found: 2609 Sort by:
  • Deafness, Autosomal Recessive 59
    OMIM # 610220
    DFNB59
  • Neurodegeneration with Brain Iron Accumulation 2B
    OMIM # 610217
    NBIA2B, Neurodegeneration with Brain Iron Accumulation, PLA2G6-Related, Neuroaxonal Dystrophy, Atypical
  • Deafness, Autosomal Recessive 66
    OMIM # 610212
    DFNB66
  • Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism
    OMIM # 610199
    NDH, NDH Syndrome,
  • Joubert Syndrome 5
    OMIM # 610188
    JBTS5
  • Microphthalmia, Isolated 2
    OMIM # 610093
    MCOP2, Anophthalmia, Clinical, Isolated
  • Short Stature and Facioauriculothoracic Malformations
    OMIM # 609654
  • Majeed Syndrome
    OMIM # 609628
    Chronic Recurrent Multifocal Osteomyelitis, Congenital Dyserythropoietic Neutrophilic Dermatosis
  • Joubert Syndrome 4
    OMIM # 609583
    JBTS4
  • Mitochondrial DNA Depletion Syndrome 2 (Myopathic Type)
    OMIM # 609560
    MTDPS2, Mitochondrial DNA Depletion Myopathy, TK2-Related
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