SNOMED Clinical Terms - Hereditary hollow viscus myopathy - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

Details
Visualization
Notes ()
Term Mappings (3)
Term Resources

Preferred Name	Hereditary hollow viscus myopathy
Synonyms	Familial visceral myopathy Hereditary hollow viscus myopathy (disorder)
ID	63684002
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/63684002
CONCEPTSTATUS	0
CTV3ID	XUI18
has_associated_morphology	Degeneration Pseudo-obstruction
has_clinical_course	Courses
has_episodicity	Episodicities
has_finding_site	Muscularis propria Intestinal structure
has_severity	Severities
isa	Autosomal hereditary disorder Disorder of smooth muscle Hollow visceral myopathy Degenerative disorder Digestive system hereditary disorder
ISPRIMITIVE	1
Semantic_Type	Disease or Syndrome
SNOMEDID	D5-01032
SYNONYM FN	Hereditary hollow viscus myopathy (disorder)
SYNONYM SY	Familial visceral myopathy
TUI	T047
UMLS_CUI	C0266833

Create New Mapping

Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://www.orphanet.org/rdfns#pat_id_1209	Experimental Factor Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_1209	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/155310	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0266833	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