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CTGA Database Listing
Arab Genomic Studies
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  • Hypoparathyroidism, Sensorineural Deafness, and Renal Disease
    OMIM # 146255
    HDR Syndrome, Barakat Syndrome, Nephrosis, Nerve Deafness, and Hypoparathyroidism
  • GATA-Binding Protein 3
    OMIM # 131320
    GATA3, Enhancer-Binding Protein GATA3
  • Cyclin-Dependent Kinase Inhibitor 1C
    OMIM # 600856
    CDKN1C, p57, KIP2,
  • Beckwith-Wiedemann Syndrome
    OMIM # 130650
    BWS, EMG Syndrome, Exomphalos-Macroglossia-Gigantism Syndrome, Wiedemann-Beckwith Syndrome, WBS, Beckwith-Wiedemann Syndrome Chromosome Region, BWCR
  • Seizures, Benign Familial Neonatal, 1
    OMIM # 121200
    BFNS1, Epilepsy, Benign Neonatal, 1, and/or Myokymia, Included, Seizures, Benign Familial Neonatal, 1, and/or Myokymia
  • Potassium Channel, Voltage-Gated, KQT-Like Subfamily, Member 2
    OMIM # 602235
    KCNQ2, Potassium Channel, Voltage-Gated, Subfamily Q, Member 2
  • Glucose-6-Phosphatase, Catalytic
    OMIM # 613742
    G6PC, Glucose-6-Phosphatase, Catalytic, 1, G6PC1, G6PT
  • Solute Carrier Family 4 (Sodium Bicarbonate Cotransporter), Member 4
    OMIM # 603345
    SLC4A4, Sodium Bicarbonate Cotransporter 1, NBC1, Solute Carrier Family 4 (Sodium Bicarbonate Cotransporter), Member 5, Formerly, SLC4A5,
  • Renal Tubular Acidosis, Proximal, with Ocular Abnormalities and Mental Retardation
    OMIM # 604278
    RTA, Proximal, Autosomal Recessive
  • Usher Syndrome, Type IF
    OMIM # 602083
    USH1F,
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