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CTGA Database Listing
Arab Genomic Studies
Records found: 2872 Sort by:
  • Ectopic P-Granules Autophagy Protein 5, C. Elegans, Homolog of
    OMIM # 615068
    EPG5, KIAA1632, HEEW1,
  • Ataxia-Telangiectasia Mutated Gene
    OMIM # 607585
    ATM
  • Breast Cancer 1 Gene
    OMIM # 113705
    BRCA1
  • BRCA2 Gene
    OMIM # 600185
    BRCA2, FANCD1 Gene, FANCD1
  • Ulna and Fibula, Absence of, with Severe Limb Deficiency
    OMIM # 276820
    Limb/Pelvis-Hypoplasia/Aplasia Syndrome, LPHAS, Al-Awadi/Raas-Rothschild Syndrome, AARRS, Schinzel Phocomelia Syndrome
  • Wingless-Type MMTV Integration Site Family, Member 7A
    OMIM # 601570
    WNT7A
  • Orofaciodigital Syndrome VI
    OMIM # 277170
    Oral-Facial-Digital syndrome, Type VI, OFDS VI, Varadi-Papp Syndrome, Varadi Syndrome, Polydactyly, Cleft Lip/Palate or Lingual Lump, and Psychomotor Retardation
  • Spondylocostal Dysostosis, Autosomal Recessive, 1
    OMIM # 277300
    SCDO1, Vertebral Anomalies, Jarcho-Levin Syndrome, Spondylothoracic Dysplasia, Costovertebral Dysplasia, Spondylothoracic Dysostosis,
  • Methylmalonic Aciduria and Homocystinuria, cblC Type
    OMIM # 277400
    Methylmalonic Acidemia and Homocystinuria, cblC Type, Methylmalonic Aciduria and Homocystinuria, Vitamin B12-Responsive, Vitamin B12 Metabolic Defect with Combined Deficiency of Methylmalonyl-CoA Mutase and Homocysteine:Methyltetrahydrofolate Methyltransferase
  • Metabolism of Cobalamin Associated C
    OMIM # 609831
    MMACHC
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