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CTGA Database Listing
Arab Genomic Studies
Records found: 2410 Sort by:
  • Dedicator of Cytokinesis 8
    OMIM # 611432
    DOCK8
  • Roundabout, Drosophila, Homolog of, 3
    OMIM # 608630
    ROBO3, RB-Inhibiting Gene 1, RBIG1, RIG1
  • Gaze Palsy, Familial Horizontal, with Progressive Scoliosis
    OMIM # 607313
    HGPPS, Ophthalmoplegia, Progressive External, and Scoliosis
  • Anti-Mullerian Hormone Type II Receptor
    OMIM # 600956
    AMHR2, Anti-Mullerian Hormone Receptor, AMHR, Mullerian Inhibiting Substance Type II Receptor, MISR2,
  • Persistent Mullerian Duct Syndrome, Types I and II
    OMIM # 261550
    PMDS, Pseudohermaphroditism, Male Internal, Hernia Uteri Inguinale, Persistent Oviduct Syndrome, Female Genital Ducts in otherwise Normal Male, Mullerian Derivatives, Persistent,
  • Hyperimmunoglobulin E-Recurrent Infection Syndrome, Autosomal Recessive
    OMIM # 243700
    Hyper-IgE Syndrome, Autosomal Recessive, HIES, Autosomal Recessive
  • Glaucoma 3, Primary Congenital, A
    OMIM # 231300
    GLC3A, Glaucoma, Congenital, GLC3, Buphthalmos
  • Adrenal Hyperplasia, Congenital, due to 21-Hydroxylase Deficiency
    OMIM # 201910
    Adrenal Hyperplasia III, 21-@Hydroxylase Deficiency, CYP21 Deficiency, Congenital Adrenal Hyperplasia 1, CAH1, Cytochrome P450, Subfamily XXIA, Polypeptide 2, CYP21A2, Cytochrome P450, Subfamily XXI, CYP21, Steroid Cytochrome P450 21-Hydroxylase, P450c21, 21-@Hydroxylase B, Included, CYP21B, CA21H, Cytochrome P450, Subfamily XXIA, Polypeptide 1 Pseudogene, CYP21A1P, CYP21P, CYP21A, Hyperandrogenism, Nonclassic Type, Due To 21-Hydroxylase Deficiency
  • DDB1- and CUL4-Associated Factor 17
    OMIM # 612515
    DCAF17, Chromosome 2 Open Reading Frame 37, C2ORF37
  • Thrombophilia Due to Protein C Deficiency, Autosomal Recessive
    OMIM # 612304
    THPH4, Protein C Deficiency, Autosomal Recessive, PROC Deficiency, Autosomal Recessive,
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