_:vb50936830 . _:vb50936831 . _:vb50936831 . . "OMIM mapping confirmed by DO. [SN]."^^ . "UMLS_CUI:C1563715"^^ . _:vb50936831 . "OMIM:170390"^^ . "ORDO:37553"^^ . _:vb50936830 . "disease_ontology"^^ . . . _:vb50936831 . "Andersen-Tawil syndrome"^^ . "Long QT syndrome 7"@en . "ANDERSEN CARDIODYSRHYTHMIC PERIODIC PARALYSIS"@en . "GARD:9453"^^ . "A long QT syndrome that has_material_basis_in autosomal dominant inheritance of a mutation in the KCNJ2 gene which disrupts the rhythm of the heart's lower chambers (ventricular arrhythmia) and results_in an unusually small lower jaw (micrognathia), low-set ears, and an abnormal curvature of the fingers called clinodactyly."^^ . . _:vb50936830 . "NCI:C84559"^^ . "LQT7"@en . "SNOMEDCT_US_2021_09_01:422348008"^^ . "DOID:0050434"^^ . "MESH:D050030"^^ . _:vb50936831 . . "Potassium-Sensitive Cardiodysrhythmic Type"@en . _:vb50936830 . _:vb50936830 . "Andersen syndrome"@en .