About: factor VIII deficiency

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An Entity of Type : owl:Class, within Data Space : demo.openlinksw.com associated with source document(s)

OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	X-linked recessive disease blood coagulation disease nodeID://b50948178
label	factor VIII deficiency
comment	OMIM mapping confirmed by DO. [SN].
has exact match	MESH:D006467
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:12134
database_cross_reference	GARD:6591 ICD10CM:D66 ICD9CM:286.0 MESH:D006467 NCI:C27146 OMIM:306700 ORDO:98878 SNOMEDCT_US_2021_09_01:28293008 UMLS_CUI:C0019069
has_exact_synonym	Congenital factor VIII disorder (en) Hemophilia A (en) Subhemophilia (en) classic hemophilia A (en)
has_obo_namespace	disease_ontology
in_subset	NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	A blood coagulation disease that has_material_basis_in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50948179

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