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CTGA Database Listing
Arab Genomic Studies
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  • Lipase H
    OMIM # 607365
    LIPH, Membrane Associated Phoshatidic Acid-Selective Phospholipase A1 , MPAPLA1, Phospholipase A1, Phosphatidic Acid-Selective, Membrane-Associated , LPD Lipase-Related Protein, LPDLR
  • Arrhythmogenic Right Ventricular Dysplasia, Familial, 11
    OMIM # 610476
    ARVD11 , Arrhythmogenic Right Ventricular Cardiomyopathy 11 , ARVC11 , Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 with Mild Palmoplantar Keratoderma with or without Woolly Hair
  • Desmocollin-2
    OMIM # 125645
    Desmocollin 3, Formerly, DSC3, Formerly, Desmosomal Glycoprotein II/III, DG2/3, DG2
  • Desmoplakin
    OMIM # 125647
    DSP, Desmoplakin I, DSPI, Desmoplakin II, DSPII
  • Psoriasis 14, Pustular
    OMIM # 614204
    PSORS14, Interleukin 36 Receptor Antagonist Deficiency, DITRA, Generalized Pustular Psoriasis, GPP, PSORP, Acrodermatitis Continua of Hallopeau, Palmoplantar Pustulosis
  • Interleukin 36 Receptor Antagonist
    OMIM # 605507
    IL36RN , Interleukin 1 Family, Member 5, IL1F5, Interleukin 1 Receptor Antagonist Homolog 1 , IL1HY1, Family of Interleukin 1-Delta , FIL1-Delta, IL1RP3
  • ADP Ribosylation Factor-Like 2-Binding Protein
    OMIM # 615407
    ARL2BP, ARL2-Binding Protein, Binder of ARL2, BART
  • Retinitis Pigmentosa 82 with or without Situs Inversus
    OMIM # 615434
    RP82
  • Ocular Cicatricial Pemphigoid
    OMIM # 164185
    OCP
  • Oculocerebrocutaneous Syndrome
    OMIM # 164180
    OCCS, Orbital Cyst with Cerebral and Focal Dermal Malformations, Delleman Syndrome, Leichtman-Wood-Rohn syndrome
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