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CTGA Database Listing
Arab Genomic Studies
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  • Twist Family bHLH Transcription Factor 2
    OMIM # 607556
    TWIST2, Twist, Drosophila, Homolog of, 2, Dermis-Expressed Protein 1, Mouse, Homolog of, Dermo1,
  • Focal Facial Dermal Dysplasia 3, Setleis Type
    OMIM # 227260
    FFDD3, Setleis Syndrome, Bitemporal Forceps Marks Syndrome, Facial Ectodermal Dysplasia, Focal Facial Dermal Dysplasia, Type II
  • Lissencephaly I
    OMIM # 607432
    LIS1 , Lissencephaly Sequence, Isolated, ILS, Lissencephaly, Classic, Subcortical Laminar Heterotopia, SCLH, Subcortical Band Heterotopia, SBH,
  • SRY-Box 18
    OMIM # 601618
    SOX18
  • Hypotrichosis-Lymphedema-Telangiectasia Syndrome
    OMIM # 607823
    HLTS
  • Joubert Syndrome 2
    OMIM # 608091
    JBTS2, Cerebellooculorenal Syndrome 2, CORS2,
  • 1-@Acylglycerol-3-Phosphate O-Acyltransferase 2
    OMIM # 603100
    AGPAT2 , Lysophosphatidic Acid Acyltransferase-Beta, LPAAT-Beta,
  • Lipodystrophy, Congenital Generalized, Type 1
    OMIM # 608594
    CGL1, Berardinelli-Seip Congenital Lipodystrophy, Type 1, BSCL1, Lipodystrophy, Berardinelli-Seip Congenital, Type 1, Brunzell Syndrome, AGPAT2-Related,
  • Sulfite Oxidase
    OMIM # 606887
    SUOX
  • Sulfocysteinuria
    OMIM # 272300
    Sulfite Oxidase Deficiency
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