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CTGA Database Listing
Arab Genomic Studies
Records found: 2557 Sort by:
  • 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
  • Thyrotoxic Periodic Paralysis, Susceptibility to, 1
    OMIM # 188580
    TTPP1, Hashitoxic Periodic Paralysis
  • DiGeorge Syndrome
    OMIM # 188400
    DGS, Chromosome 22q11.2 Deletion Syndrome, Hypoplasia of Thymus and Parathyroids, Third and Fourth Pharyngeal Pouch Syndrome, Digeorge Syndrome Chromosome Region, DGCR, Takao VCF Syndrome, Catch22
  • Thrombocytopenic Purpura, Autoimmune
    OMIM # 188030
    AITP, Immune Thrombocytopenic Purpura, Idiopathic Thrombocytopenic Purpura, ITP
  • Thanatophoric Dysplasia, Type I
    OMIM # 187600
    TD, TD1, Lethal Short-Limbed Platyspondylic Dwarfism, San Diego Type, Platyspondylic Lethal Skeletal Dysplasia, San Diego Type, Thanatophoric Dwarfism, Thanatophoric Dysplasia
  • Tetralogy of Fallot
    OMIM # 187500
    TOF
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