About: platelet-type bleeding disorder 16

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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 blood platelet disease nodeID://b50939210 nodeID://b50939211
label	platelet-type bleeding disorder 16
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060691
database_cross_reference	ICD10CM:D69.4 OMIM:187800 ORDO:140957
has_exact_synonym	autosomal dominant thrombasthenia of Glanzmann and Naegeli (en) autosomal dominant Glanzmann thrombasthenia (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A blood platelet disease characterized by autosomal dominant inheritance with macrothrombocytopenia, platelet anisocytosis, prolonged bleeding time but only mildly increased bleeding tendency that has material basis_in heterozygous mutation in the ITGA2B gene on chromosome 17q21.31 or the ITGB3 gene on chromosome 17q21.32.
is first of	nodeID://b50956986
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50939212

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