. _:vb50944617 . . _:vb50944618 . _:vb50944619 . "dominant optic atrophy plus syndrome"^^ . "DOA+"@en . _:vb50944616 . _:vb50944619 . _:vb50944618 . _:vb50944618 . _:vb50944619 . _:vb50944617 . "UMLS_CUI:C3276549"^^ . _:vb50944617 . . _:vb50944616 . _:vb50944616 . _:vb50944617 . _:vb50944616 . "disease_ontology"^^ . "DOID:0111340"^^ . _:vb50944617 . "GARD:5243"^^ . _:vb50944618 . _:vb50944619 . _:vb50944616 . "A syndrome characterized by visual loss and sensorineural hearing loss with onset in childhood and associated with other symptoms including; progressive external ophthalmoplegia, muscle cramps, hyperreflexia, and ataxia that has_material_basis_in heterozygous mutation in OPA1 on chromosome 3q29."^^ . . "OMIM:125250"^^ . "optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy"@en . _:vb50944619 . _:vb50944618 .