About: congenital afibrinogenemia

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	autosomal recessive disease physical disorder blood coagulation disease nodeID://b50950647 nodeID://b50950648
label	congenital afibrinogenemia
comment	OMIM mapping confirmed by DO. [SN].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:2236
database_cross_reference	GARD:5761 MESH:D000347 NCI:C98130 OMIM:202400 SNOMEDCT_US_2021_09_01:278504009 UMLS_CUI:C0001733
has_exact_synonym	Factor I deficiency (en) Fibrinogen deficiency (en)
has_obo_namespace	disease_ontology
in_subset	NCIthesaurus
http://purl.obolib...g/obo/IAO_0000115	A blood coagulation disease that is characterized by an impaired blood clotting resulting from a lack deficiency of a the fibrinogen protein (coagulation factor I).
is first of	nodeID://b50956967
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50950649

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