About: autosomal dominant sensory ataxia 1

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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 hereditary ataxia nodeID://b50944353
label	autosomal dominant sensory ataxia 1
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0111170
database_cross_reference	OMIM:608984
has_exact_synonym	ADSA (en) SNAX1 (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A hereditary ataxia characterized by gait difficulty and instability especially in dark conditions resulting from sensory loss in the extremities and without cerebellar involvement that has_material_basis_in heterozygous mutations in the RNF170 gene on chromosome 8.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50944354

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