SNOMED Clinical Terms - Amyotrophia congenita - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Amyotrophia congenita
Synonyms	Amyotrophia congenita (disorder)
ID	75491005
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/75491005
CONCEPTSTATUS	0
CTV3ID	XUKLe
has_associated_morphology	Congenital hypoplasia Congenital atrophy
has_clinical_course	Courses
has_finding_site	Skeletal muscle structure
has_severity	Severities
isa	Congenital malformation Hypoplasia of muscle Muscle atrophy Congenital anomaly of skeletal muscle
ISPRIMITIVE	1
occurs_in	Congenital
same_as	Amyotrophica congenita
Semantic_Type	Congenital Abnormality
SNOMEDID	D4-10520
SYNONYM FN	Amyotrophia congenita (disorder)
TUI	T019
UMLS_CUI	C0265520

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://uwhealth.org/himc/icd/icd09/#756.89	ICD09	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q79.8	ICD10CM	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/PGyy0	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0265520	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q79.8	ICD10CM	NLM UMLS (CUI)	CUI: C0265520	skos:closeMatch	loom	04/02/13	View Notes

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