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CTGA Database Listing
Arab Genomic Studies
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  • 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
  • Cholinergic Receptor, Neuronal Nicotinic, Beta Polypeptide 2
    OMIM # 118507
    CHRNB2, Acetylcholine Receptor, Neuronal Nicotinic, Beta-2 Subunit
  • Epilepsy, Nocturnal Frontal Lobe, 3
    OMIM # 605375
    ENFL3
  • Cornelia de Lange Syndrome 4
    OMIM # 614701
    CDLS4
  • Rad21, S. Pombe, Homolog of
    OMIM # 606462
    RAD21
  • 3-@Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase (*)
    OMIM # 607764
    HSD3B7
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