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CTGA Database Listing
Arab Genomic Studies
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  • Lymphedema-Distichiasis Syndrome
    OMIM # 153400
    Lymphedema with Distichiasis, Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus
  • Dislocated Elbows, Bowed Tibias, Scoliosis, Deafness, Cataract, Microcephaly, and Mental Retardation
    OMIM # 603133
  • Dihydropyrimidinase Deficiency
    OMIM # 222748
    DPYSD, Dihydropyrimidinuria, DPYS Deficiency, DPH Deficiency
  • Dihydropyriminidase
    OMIM # 613326
    DPYS, 5,6-Dihydropyrimidine Amidohydrolase, DHP, Hydantoinase,
  • 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
  • Diastrophic Dysplasia
    OMIM # 222600
    DTD, DD, DIiastrophic Dysplasia, Broad Bone-Platyspondylic Variant
  • Solute Carrier Family 26 (Sulfate Transporter), Member 2
    OMIM # 606718
    SLC26A2, DTD Sulfate Transporter, DTDST
  • Vibratory Urticaria
    OMIM # 125630
    VBU, Dermodistortive Urticaria, DDU, Vibratory Angioedema
  • Adhesion G Protein-Coupled Receptor E2
    OMIM # 606100
    ADGRE2, EGF-Like Module-Containing, Mucin-Like Hormone Receptor 2, EMR2,
  • Cohen Syndrome
    OMIM # 216550
    COH1, CHH1, Hypotonia Obesity and Prominent Incisors, Pepper Syndrome, CHS1
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