SNOMED Clinical Terms - Congenital fibrinogen abnormality - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

Details
Visualization
Notes ()
Term Mappings (2)
Term Resources

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

Create New Mapping

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	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X20EW	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0398616	skos:closeMatch	loom	04/02/13	View Notes

Map From

Map To

advanced options

The National Center for Biomedical Ontology is one of the National Centers for Biomedical Computing supported by the NHGRI, the NHLBI, and the NIH Common Fund under grant U54-HG004028.
Copyright © 2005‑2013, The Board of Trustees of Leland Stanford Junior University. All rights reserved.
NCBO Website Release Notes Terms of Use Privacy Policy How to Cite