_:vb50942152 . _:vb50942151 . "DOID:0090045"^^ . "OMIM:612126"^^ . . "ORDO:98811"^^ . . . "disease_ontology"^^ . "A dystonia that is characterized by paroxysmal exercise-induced dyskinesia involving transient abnormal involuntary movements in the exercised limbs, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34."^^ . _:vb50942152 . _:vb50942151 . _:vb50942151 . _:vb50942152 . _:vb50942151 . _:vb50942151 . _:vb50942152 . _:vb50942152 . "childhood onset GLUT1 deficiency syndrome 2"^^ . "ICD10CM:G24.8"^^ . .