SNOMED Clinical Terms - Hereditary myositis ossificans - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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

Preferred Name	Hereditary myositis ossificans
Synonyms	Hereditary myositis ossificans (disorder)
ID	240088005
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/240088005
CONCEPTSTATUS	0
CTV3ID	X7095
has_associated_morphology	Osseous metaplasia
has_clinical_course	Courses
has_episodicity	Episodicities
has_finding_site	Skeletal muscle structure
has_severity	Severities
isa	Disorder of skeletal muscle Muscular ossification Hereditary disorder of musculoskeletal system Soft tissue lesion
ISPRIMITIVE	1
Semantic_Type	Congenital Abnormality Disease or Syndrome
SNOMEDID	DA-51506
SYNONYM FN	Hereditary myositis ossificans (disorder)
TUI	T019 T047
UMLS_CUI	C0410208

Create New Mapping

Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/RCD/X7095	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/X7095	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0410208	skos:closeMatch	loom	05/21/13	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