SNOMED Clinical Terms - Pseudo von Willebrand disease - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Pseudo von Willebrand disease
Synonyms	Pseudo von Willebrand disease (disorder)
Definitions	Any inherited disorder mimicking von Willebrand disease but lacking mutation at the VWF locus
ID	128115005
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/128115005
CONCEPTSTATUS	0
CTV3ID	XU76G
has_clinical_course	Courses
has_episodicity	Episodicities
has_severity	Severities
isa	Blood coagulation disorder Autosomal dominant hereditary disorder
ISPRIMITIVE	1
Semantic_Type	Disease or Syndrome
SNOMEDID	DC-64211
SYNONYM FN	Pseudo von Willebrand disease (disorder)
TUI	T047
UMLS_CUI	C1280798

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://www.orphanet.org/rdfns#pat_id_10700	Experimental Factor Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X20Es	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C1280798	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/C536458	Medical Subject Headings (MeSH)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/177820	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C1280798	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/C536458	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C1280798	skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_10700	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/177820	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes

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