SNOMED Clinical Terms - Manifesting female carrier of X-linked muscular dystrophy - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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

Preferred Name	Manifesting female carrier of X-linked muscular dystrophy
Synonyms	Manifesting female carrier of X-linked muscular dystrophy (disorder)
ID	240050008
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/240050008
CONCEPTSTATUS	0
CTV3ID	X708L
has_associated_morphology	Congenital anomaly Dystrophy
has_clinical_course	Courses
has_finding_site	Skeletal muscle structure
has_severity	Severities
isa	X-linked muscular dystrophy with abnormal dystrophin
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Disease or Syndrome
SNOMEDID	DA-51119
SYNONYM FN	Manifesting female carrier of X-linked muscular dystrophy (disorder)
TUI	T047
UMLS_CUI	C0410167

Create New Mapping

Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/RCD/X708L	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X708L	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0410167	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