SNOMED Clinical Terms - Mietens syndrome - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Mietens syndrome
Synonyms	Mietens syndrome (disorder)
ID	40291001
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/40291001
CONCEPTSTATUS	0
CTV3ID	XUDNn
has_associated_morphology	Congenital malformation
has_clinical_course	Courses
has_finding_site	Limb structure
has_severity	Severities
isa	Multiple malformation syndrome with facial-limb defects as major feature
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Congenital Abnormality Disease or Syndrome
SNOMEDID	D4-00807
SYNONYM FN	Mietens syndrome (disorder)
TUI	T019 T047
UMLS_CUI	C0265249

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/MSH/C537444	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C0265249	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/249600	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0265249	skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_2360	Experimental Factor Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_2360	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes

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