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CTGA Database Listing
Arab Genomic Studies
Records found: 2828 Sort by:
  • Transglutaminase 1
    OMIM # 190195
    TGM1, Transglutaminase, Keratinocyte, TGK, Transglutaminase, Epidermal Type I,
  • Ichthyosis, Lamellar, 1
    OMIM # 242300
    LI1, Ichthyosis Congenita, Lamellar Exfoliation of Newborn, Desquamation of Newborn, Collodion Fetus, Lamellar Ichthyosis, LI, Lamellar Ichthyosis, Type 1, Ichthyosis Congenita II, ICR2, Self-Healing Collodion Baby,
  • Anorexia Nervosa, Susceptibility to, 1
    OMIM # 606788
    ANON1, AN
  • Polymicrogyria, Bilateral Frontoparietal
    OMIM # 606854
    BFPP, Cerebellar Ataxia with Neuronal Migration Defect,
  • 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
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