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CTGA Database Listing
Arab Genomic Studies
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  • Cone-Rod Synaptic Disorder, Congenital Nonprogressive
    OMIM # 610427
    CRSD, Night Blindness, Congenital Stationary, Type 2B, CSNB2B, Night Blindness, Congenital Stationary, Incomplete, Autosomal Recessive,
  • Aicardi-Goutieres Syndrome 3
    OMIM # 610329
    AGS3
  • Deafness, Autosomal Recessive 67
    OMIM # 610265
    DFNB67
  • Kleefstra Syndrome
    OMIM # 610253
    Chromosome 9q34.3 Deletion Syndrome, 9q- Syndrome, 9q Subtelomeric Deletion Syndrome,
  • 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
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