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CTGA Database Listing
Arab Genomic Studies
Records found: 2744 Sort by:
  • 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
  • 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
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