About: myoclonic dystonia 26

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Attributes	Values
type	Class
subClassOf	autosomal dominant disease myoclonic dystonia nodeID://b50942131
label	myoclonic dystonia 26
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0090036
database_cross_reference	OMIM:616398
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A myoclonic dystonia characterized by onset of myoclonic jerks affecting the upper limbs, progressing to dystonia with predominant involvement of the craniocervical regions, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the KCTD17 gene on chromosome 22q12.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50942132

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