SNOMED Clinical Terms - Congenital fibrinogen abnormality | NCBO BioPortal

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Preferred Name	Congenital fibrinogen abnormality
Synonyms	Congenital fibrinogen abnormality (disorder)
ID	234456000
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/234456000
CONCEPTSTATUS	0
CTV3ID	X20EW
has_clinical_course	Courses
has_severity	Severities
isa	Congenital disease Fibrinogen abnormality
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Disease or Syndrome
SNOMEDID	DC-6002B
SYNONYM FN	Congenital fibrinogen abnormality (disorder)
TUI	T047
UMLS_CUI	C0398616

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/RCD/X20EW	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/X20EW	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0398616	skos:closeMatch	loom	05/21/13	View Notes

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