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CTGA Database Listing
Arab Genomic Studies
Records found: 2870 Sort by:
  • Alpha-L-Iduronidase
    OMIM # 252800
    IDUA, Iduronidase, Alpha-L
  • Hurler-Scheie Syndrome
    OMIM # 607015
    Mucopolysaccharidosis Type IH/S, MPS1-HS
  • Kinesin Family Member 7
    OMIM # 611254
    KIF7
  • Al-Gazali-Bakalinova Syndrome
    OMIM # 607131
    Macrocephaly with Multiple Epiphyseal Dysplasia and Distinctive Facies, MMEDF
  • Meckel Syndrome, Type 3
    OMIM # 607361
    MKS3, Meckel-Gruber Syndrome, Type 3
  • Transmembrane Protein 138
    OMIM # 614459
    TMEM138
  • Bartter Syndrome, Type 3
    OMIM # 607364
    Bartter Syndrome, Classic, Bartter Syndrome, Type 3, with Hypocalciuria
  • Glucocorticoid Deficiency 2
    OMIM # 607398
    GCCD2, Familial Glucocorticoid Deficiency 2, FGD2,
  • Glucocorticoid Deficiency 1
    OMIM # 202200
    GCCD1, Familial Glucocorticoid Deficiency 1, FGD1, Adrenal Unresponsiveness to ACHT, ACTH resistance
  • Patent Ductus Arteriosus
    OMIM # 607411
    PDA, PDA1
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