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CTGA Database Listing
Arab Genomic Studies
Records found: 2746 Sort by:
  • Meckel Syndrome, Type 3
    OMIM # 607361
    MKS3, Meckel-Gruber Syndrome, Type 3
  • Transmembrane Protein 67
    OMIM # 609884
    TMEM67, MKS3 Gene, MKS3, Meckelin
  • Elastosis Perforans Serpiginosa
    OMIM # 130100
    EPS, Elastoma Intrapapillare Perforans Verruciformis, Miescher Elastoma,
  • Down Syndrome
    OMIM # 190685
    Trisomy 21, DCR, Down Syndrome Chromosome Region, DSCR, Down Syndrome Critical Region, Transient Myeloproliferative Disorder of Down Syndrome, Leukemia, Megakaryoblastic, of Down Syndrome
  • Progressive Familial Heart Block, Type IB
    OMIM # 604559
    Progressive Familial Heart Block, Type IB
  • Fibromatosis, Gingival, with Hypertrichosis and Mental Retardation
    OMIM # 605400
  • Dubowitz Syndrome
    OMIM # 223370
  • Spinal Muscular Atrophy, Distal, Autosomal Recessive
    OMIM # 607088
    DSMA3, Nuronopathy, Distal Hereditary Motor, Type IV , HMN4, DHMN4, Neuropathy, Distal Hereditary Motor, Type IV, HMN IV, Neuropathy, Distal Hereditary Motor, Type III, HMN3, DHMN3, HMN III,
  • Parkinson Disease 7, Autosomal Recessive Early-Onset
    OMIM # 606324
    PARK7
  • Megarbane Syndrome
    OMIM # 606527
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