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CTGA Database Listing
Arab Genomic Studies
Records found: 2565 Sort by:
  • Camptodactyly with Muscular Hypoplasia, Skeletal Dysplasia, and Abnormal Palmar Creases
    OMIM # 211960
    Tel Hashomer Camptodactyly Syndrome
  • C Syndrome
    OMIM # 211750
    Optiz Trigonocephaly Syndrome, Trigonocephaly Syndrome,
  • Cholestasis, Progressive Familial Intrahepatic, 1
    OMIM # 211600
    PFIC1, Byler Disease, Cholestasis, Fatal Intrahepatic
  • Bronchomalacia
    OMIM # 211450
    Williams-Campbell Syndrome
  • Bronchiectasis with or without Elevated Sweat Chloride 1
    OMIM # 211400
    BESC1, Cystic Fibrosis-Like Syndrome, Atypical Cystic Fibrosis
  • Seckel Syndrome 1
    OMIM # 210600
    SCKL1, SCKL, Bird-Headed Dwarfism, Seckel-Type Dwarfism, Nanocephalic Dwarfism, Microcephalic Primordial Dwarfism I
  • Bardet-Biedl Syndrome 1
    OMIM # 209900
    BBS1,
  • 3-@Methylcrotonyl-CoA Carboxylase 1 Deficiency
    OMIM # 210200
    MCCD Type 1, MCC1 Deficiency, 3-Methylcrotonylglycinuria I, Methylcrotonylglycinuria Type I
  • Central Hypoventilation Syndrome, Congenital
    OMIM # 209880
    CCHS, Autonomic Control, Congenital Failure of, Ondine Curse, Congenital, Ondine-Hirschsprung Disease, OHD, CCHS with Hirschsprung Disease, Haddad Syndrome
  • Autism
    OMIM # 209850
    Autistic Disorder, Autism, susceptibility 1, AUTS1, Autism Spectrum Disorder
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