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CTGA Database Listing
Arab Genomic Studies
Records found: 2804 Sort by:
  • Citrullinemia, Classic
    OMIM # 215700
    Citrullinemia, Type I, CTLN1, Citrullinuria, Argininosuccinate Synthetase Deficiency, ASS Deficiency
  • ALG9, S. Cerevisiae, Homolog of
    OMIM # 606941
    Disrupted in Bipolar Disorder 1, DIBD1,
  • Congenital Disorder of Glycosylation, Type Il
    OMIM # 608776
    CDG Il, CDG1L, ALG9-CDG,
  • Titin
    OMIM # 188840
    TTN, Connectin
  • Cardiomyopathy, Dilated, 1G
    OMIM # 604145
    CMD1G
  • 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
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