SNOMED Clinical Terms - Hereditary oculoleptomeningeal amyloid angiopathy - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Hereditary oculoleptomeningeal amyloid angiopathy
Synonyms	Amyloidosis VII Ohio type amyloidosis Familial oculoleptomeningeal amyloidosis Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
ID	43532007
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/43532007
CONCEPTSTATUS	0
CTV3ID	X40Ps
has_associated_morphology	Focal amyloid
has_clinical_course	Courses
has_episodicity	Episodicities
has_finding_site	Leptomeninges structure Blood vessel structure
has_severity	Severities
isa	Disorder of meninges Hereditary disorder of nervous system Vascular disorder Localized amyloidosis Cardiovascular system hereditary disorder Autosomal dominant hereditary disorder
ISPRIMITIVE	1
Semantic_Type	Disease or Syndrome
SNOMEDID	D6-94620
SYNONYM FN	Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
SYNONYM SY	Amyloidosis VII Ohio type amyloidosis Familial oculoleptomeningeal amyloidosis
TUI	T047
UMLS_CUI	C0342609

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/RCD/X40Ps	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0342609	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X40Ps	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes

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