SNOMED Clinical Terms - Congenital fascial dystrophy - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Congenital fascial dystrophy
Synonyms	Congenital fascial dystrophy (disorder)
ID	399948007
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/399948007
CONCEPTSTATUS	0
CTV3ID	XUYy6
has_associated_morphology	Fibrosis Degeneration
has_clinical_course	Courses
has_finding_site	Skin structure
has_severity	Severities
inverse_may_be_a	Infantile stiff skin syndrome
isa	Congenital disease Infantile stiff skin syndrome
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Congenital Abnormality Disease or Syndrome
SNOMEDID	D0-00193
SYNONYM FN	Congenital fascial dystrophy (disorder)
TUI	T019 T047
UMLS_CUI	C1302740

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/OMIM/228020	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C1302740	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/X50DS	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C1302740	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/X50DS	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes

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