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Metadata
ID	DOID:0090048
Name	dystonia 16
Definition	A multifocal dystonia that is characterized by early-onset progressive limb dystonia, laryngeal and oromandibular dystonia, and parkinsonism, and that has_material_basis_in autosomal recessive inheritance of homozygous mutation in the protein activator of interferon induced protein kinase EIF2AK2 (PRKRA) gene on chromosome 2q31. https://www.ncbi.nlm.nih.gov/pubmed/29279192, https://www.omim.org/entry/612067, https://www.ncbi.nlm.nih.gov/pubmed/28283962
Xrefs	GARD:10539 ICD10CM:G24.1 MESH:C567430 MIM:612067 ORDO:210571
Subsets	DO_rare_slim
Parent Relationships	is_a multifocal dystonia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance