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CTGA Database Listing
Arab Genomic Studies
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  • Diabetes Mellitus, Transient Neonatal, 1
    OMIM # 601410
    TNDM1, TNDM, DMTN
  • Insulin
    OMIM # 176730
    INS, Proinsulin
  • Larsen Syndrome, Autosomal Dominant
    OMIM # 150250
    LRS1
  • GDNF-Inducible Zinc Finger Protein 1
    OMIM # 613842
    GZF1, Zinc Finger Protein 336 , ZNF336
  • Colony-Stimulating Factor 2 Receptor, Alpha
    OMIM # 306250
    CSF2RA, Granulocyte-Macrophage Colony-Stimulating Factor Receptor, Low Affinity, Alpha Subunit, GMCSFR
  • Surfactant Metabolism Dysfunction, Pulmonary, 4
    OMIM # 300770
    SMDP4, Pulmonary Alveolar Proteinosis, Congenital, 4, PAP due to CSF2RA Deficiency, CSF2RA Deficiency
  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 3
    OMIM # 614021
    CPVT3
  • Trans-2,3-Enoyl-CoA Reductase-Like Protein
    OMIM # 617242
    TECRL, TECR-Like Protein, TER-Like Protein, TERL, Steroid 5-Alpha-Reductase 2-Like 2, SRD5A2L2, GPSN2-Like, GPSN2L
  • Clarin 1
    OMIM # 606397
    CLRN1, USH3A Gene, USH3A, USH3
  • Usher Syndrome, Type IIIA
    OMIM # 276902
    USH3A, Usher Syndrome, Type III, USH3
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