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CTGA Database Listing
Arab Genomic Studies
Records found: 2746 Sort by:
  • Quinoid Dihydropteridine Reductase
    OMIM # 612676
    QDPR, Dihydropteridine Reductase, DHPR
  • Hemifacial Microsomia
    OMIM # 164210
    HFM, Oculoauriculovertebral Spectrum, OAVS, Goldenhar Syndrome, Oculoauriculovertebral Dysplasia, OAV Dysplasia, Facioauriculovertebral Sequence, FAV Sequence
  • Low Density Lipoprotein Receptor Adaprtor Protein 1
    OMIM # 605747
    LDLRAP1, LDLR Adaptor Protein 1, ARH Gene, ARH,
  • Hypercholesterolemia, Familial, 1
    OMIM # 143890
    FHCL1, FHC, FH, Hyperlipoproteinemia, Type II, Hyperlipoproteinemia, Type IIA, Hyper-Low-Density-Lipoproteinemia, Hypercholesterolemic Xanthomatosis, Familial, LDL Receptor Disorder
  • Adams-Oliver Syndrome 2
    OMIM # 614219
    AOS2
  • 5,10-@Methylenetetrahydrofolate Reductase
    OMIM # 607093
    MTHFR
  • Internal Carotid Artery, Spontaneous Dissection of
    OMIM # 147820
  • Low Density Lipoprotein Receptor
    OMIM # 606945
    LDLR
  • Natriuretic Peptide Receptor 2
    OMIM # 108961
    NPR2; , Guanylate Cyclase B; , GCB; , GUC2B; , GUCY2B; , Atrial Natriuretic Peptide Receptor, Type B;, ANPRB; , Atrionatriuretic Peptide Receptor, Type B; , NPRB; , ANPB Receptor,
  • Acromesomelic Dysplasia, Maroteaux Type
    OMIM # 602875
    AMDM, St. Helena Dysplasia
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