About: platelet-type bleeding disorder 19

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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://b50944122
label	platelet-type bleeding disorder 19
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0111048
database_cross_reference	ICD10CM:D69.4 OMIM:616176 ORDO:438207
has_exact_synonym	BDPLT19 (en) severe autosomal recessive macrothrombocytopenia (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A blood platelet disease characterized by autosomal recessive inheritance of epistaxis, spontaneous hematomas, severe thrombocytopenia, menorrhagia, ovarian cyst ruptures, and abnormal megakaryocytic clusters that has_material_basis_in homozygous mutation in the PRKACG gene on chromosome 9q21.
is first of	nodeID://b50956980
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50944123

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