About: platelet-type bleeding disorder 9

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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://b50944114
label	platelet-type bleeding disorder 9
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0111045
database_cross_reference	ICD10CM:D69.8 OMIM:614200 ORDO:98886
has_exact_synonym	BDPLT9 (en) GP Ia deficiency (en) collagen platelet receptor deficiency (en) glycoprotein Ia deficiency (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A blood platelet disease characterized by autosomal dominant inheritance of mild thrombocytopenia, mild alpha-granue deficiency, defective platelet adhesion that has_material_basis_in mutation in the ITGA2 gene on chromosome 5q11.2.
is first of	nodeID://b50956983
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50944115

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