SNOMED Clinical Terms - Benign congenital myopathy - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Benign congenital myopathy
Synonyms	Benign congenital myopathy (disorder)
ID	193222002
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/193222002
CONCEPTSTATUS	0
CTV3ID	F3900
has_associated_morphology	Dystrophy
has_clinical_course	Courses
has_finding_site	Skeletal muscle structure
has_severity	Severities
isa	Congenital disease Muscular dystrophy
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Disease or Syndrome
SNOMEDID	DA-51101
SYNONYM FN	Benign congenital myopathy (disorder)
TUI	T047
UMLS_CUI	C0699741

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/RCD/F3900	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0699741	skos:closeMatch	loom	05/21/13	View Notes
http://www.owl-ontologies.com/NPOntology.owl#DOID_9883	Natural Products Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.obolibrary.org/obo/DOID_9883	Human disease ontology	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/F3900	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://uwhealth.org/himc/icd/icd09/#359.0	ICD09	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/CSP/0725-6597	CRISP Thesaurus, 2006	NLM UMLS (CUI)	CUI: C0699741	skos:closeMatch	loom	05/21/13	View Notes

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