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CTGA Database Listing
Arab Genomic Studies
Records found: 2115 Sort by:
  • Femoral-Facial Syndrome
    OMIM # 134780
    FFS, Femoral Hypoplasia-Unusual Facies Syndrome, FHUFS,
  • Tumor Necrosis Factor Receptor Superfamily, Member 6
    OMIM # 134637
    TNFRSF6, Apoptosis Antigen 1, APT1, FAS Antigen, Surface Antigen APO1, APO1, CD95
  • Factor XIII, B Subunit
    OMIM # 134580
    F13B, Fibrin Stabilizing Factor, B Subunit, FSF, B Subunit, Factor XIII, B Subunit, Deficiency of
  • Factor XIII, A1 Subunit
    OMIM # 134570
    F13A1, F13A, Fibrin Stabilizing Factor, A Subunit, FSF, A Subunit, Fibrinoligase, Transglutaminase, Plasma,
  • Complement Factor H
    OMIM # 134370
    CFH, H Factor 1, HF1, Factor H, HF, Factor H-Like 1, FHL1, Complement Factor H-Like 1, CFHL1
  • Exudative Vitreoretinopathy 1
    OMIM # 133780
    EVR1, Exudative Vitreoretinopathy, Familial, Autosomal Dominant, FEVR, Autosomal Dominant, Criswick-Schepens Syndrome, Retinopathy of Prematurity, ROP
  • Ewing Sarcoma Breakpoint Region 1
    OMIM # 133450
    EWSR1, EWS Gene, EWS, Ewing Sarcoma, EWS, ES, Neuroepithelioma, Peripheral, PNE, Askin Tumor, Esthesioneuroblastoma, EWS/FEV Fusion Gene, EWS/ZNF278 Fusion Gene, EWS/FLI1 Fusion Gene, EWS/ATF1 Fusion Gene, EWS/ERG Fusion Gene, EWS/WT1 Fusion Gene, EWS/CREB1 Fusion Gene, EWS/NR4A3 Fusion Gene, EWS/POU5F1 Fusion Gene, EWS/ETV1 Fusion Gene, EWS/ETV4 Fusion Gene
  • Estrogen Receptor 1
    OMIM # 133430
    ESR1, Estrogen Receptor, ESR, ER, Estrogen Receptor, Alpha, ESRA
  • Esophageal Cancer
    OMIM # 133239
    Esophageal Squamous Cell Carcinoma, ESCC
  • Erythrokeratodermia Variabilis
    OMIM # 133200
    EKV, Erythrokeratodermia Figurata, Congenital Familial, in Plaques, Erythrokeratodermia Variabilis with Erythema Gyratum Repens, Greither Disease, Keratosis Palmoplantaris Transgrediens et Progrediens, Mendes da Costa syndrome,
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