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CTGA Database Listing
Arab Genomic Studies
Records found: 2746 Sort by:
  • Dedicator of Cytokinesis 8
    OMIM # 611432
    DOCK8
  • Spinal Muscular Atrophy, Distal, Autosomal Recessive, 1
    OMIM # 604320
    DSMA1, Spinal Muscular Atrophy with Respiratory Distress 1, SMARD1, Neuronopathy, Distal Hereditary Motor, Type VI, DHMN6, HMN6, HMN VI, Severe Infantile Axonal Neuropathy with Respiratory Failure, SIANRF, Neuronopathy, Severe Infantile Axonal, with Repiratory Failure, Spinal Muscular Atrophy, Diaphragmatic
  • Immunoglobulin MU Binding Protein 2
    OMIM # 600502
    IGHMBP2, Cardiac Transcription Factor 1, CATF1, SMUBP2,
  • ATPase, Cu(2+)-Transporting, Beta Polypeptide
    OMIM # 606882
    ATP7B
  • Deafness, Autosomal Recessive 14
    OMIM # 603678
    DFNB14
  • Engulfment and Cell Motility Gene 2
    OMIM # 606421
    ELMO2, CED12, C. elegans, Homolog of, 2
  • Ramon Syndrome
    OMIM # 266270
    Cherubism, Gingival Fibromatosis, Epilepsy, Mental Deficiency, Hypertrichosis, and Stunted Growth
  • Laminin, Beta-3
    OMIM # 150310
    LAMB3, Laminin B3, Laminin 5, Beta-3 Subunit, Lam5, Beta-3 Subunit
  • C2 Calcium-Dependent Domain-Containing Protein 3
    OMIM # 615944
    C2CD3,
  • Orofaciodigital Syndrome XIV
    OMIM # 615948
    OFD14,
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