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CTGA Database Listing
Arab Genomic Studies
Records found: 2565 Sort by:
  • Interleukin 10 Receptor, Alpha
    OMIM # 146933
    IL10RA, Interleukin 10 Receptor, IL10R, IL10R1,
  • Immunodeficiency 56
    OMIM # 615207
    IMD56, IL21R Immunodeficiency,
  • Interleukin 21 Receptor
    OMIM # 605383
    IL21R, IL21R/BCL6 Fusion Gene,
  • Atrial Septal Defect 7 with or without Atrioventricular Conduction Defects
    OMIM # 108900
    ASD7 , ASD with or without Atrioventricular Conduction Defects
  • NK2 Homeobox 5
    OMIM # 600584
    NKX2-5 , NK2, Drosophila, Homolog of, E , NKX2E, Cardiac-Specific Homeobox 1, CSX1, CSX, NKX2.5, Mouse, Homolog of
  • Spinocerebellar Ataxia, Autosomal Recessive 2
    OMIM # 213200
    SCAR2, Cerebelloparenchymal Disorder III, CPD III, CPD3, Cerebellar Hypoplasia, Nonprogressive Norman Type, Cerebellar Granular Cell Hypoplasia and Mental Retardation, Congenital
  • Peptidase, Mitochondrial Processing, Alpha
    OMIM # 613036
    PMPCA , Mitochondrial Processing Peptidase-Alpha , KIAA0123
  • Tracheoesophageal Fistula with or without Esophageal Atresia
    OMIM # 189960
    Esophageal Atresia with or without Tracheoesophageal Fistula
  • Preeclampsia/Eclampsia 1
    OMIM # 189800
    PEE1, PREG1, PEE, Toxemia of Pregnancy, Hypertension, Pregnancy-Induced
  • Tibia, Hypoplasia or Aplasia of, with Polydactyly
    OMIM # 188740
    THYP, Tibial Hemimelia-Polydactyly-Triphalangeal-Thumbs with Fibular Dimelia
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