About: platelet-type bleeding disorder 8

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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 recessive disease blood platelet disease nodeID://b50939213 nodeID://b50939214
label	platelet-type bleeding disorder 8
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0060692
database_cross_reference	ICD10CM:D69.8 OMIM:609821 ORDO:36355
has_exact_synonym	ADP platelet receptor P2Y12 defect (en) P2Y12 defect (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A blood platelet disease characterized by mild to moderate mucocutaneous bleeding and absence of adenosine phosphate induced platelet aggregation that has_material_basis_in homozygous or compound heterozygous mutation in the P2RY12 gene on chromosome 3q.
is first of	nodeID://b50956985
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50939215

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