SNOMED Clinical Terms - Metachromatic leukodystrophy, congenital type - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Metachromatic leukodystrophy, congenital type
Synonyms	Metachromatic leucodystrophy, congenital type Metachromatic leukodystrophy, congenital type (disorder)
ID	40802007
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/40802007
CONCEPTSTATUS	0
CTV3ID	XUDUp
has_clinical_course	Courses
has_severity	Severities
isa	Congenital disease Metachromatic leukodystrophy
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Disease or Syndrome
SNOMEDID	D6-74410
SYNONYM FN	Metachromatic leukodystrophy, congenital type (disorder)
SYNONYM PTGB	Metachromatic leucodystrophy, congenital type
TUI	T047
UMLS_CUI	C0751278

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/RCD/X40VL	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0751278	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/250100	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0751278	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/D007966	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C0751278	skos:closeMatch	loom	04/02/13	View Notes

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