SNOMED Clinical Terms - Congenital microgastria - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Congenital microgastria
Synonyms	Congenital gastric hypoplasia Microgastria Congenital small stomach Congenital microgastria (disorder)
ID	83714006
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/83714006
CONCEPTSTATUS	0
CTV3ID	PA76.
has_associated_morphology	Congenital hypoplasia Congenital smallness
has_clinical_course	Courses
has_finding_site	Stomach structure
has_severity	Severities
isa	Congenital anomaly of abdomen Congenital anomaly of gastrointestinal tract Congenital anomaly of body cavity Congenital anomaly of stomach Congenital malformation of upper alimentary tract
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Congenital Abnormality
SNOMEDID	D4-55529
SYNONYM FN	Congenital microgastria (disorder)
SYNONYM SY	Congenital gastric hypoplasia Microgastria Congenital small stomach
TUI	T019
UMLS_CUI	C0266150

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/RCD/PA76.	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0266150	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/PA76.	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.obolibrary.org/obo/HP_0100841	Human Phenotype Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#sgn_id_26300	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_18391	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_18391	Experimental Factor Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU017166	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU017166	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0266150	skos:closeMatch	loom	04/02/13	View Notes
http://purl.org/obo/owl/HP#HP_0100841	Bone Dysplasia Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q40.2	ICD10CM	NLM UMLS (CUI)	CUI: C0266150	skos:closeMatch	loom	04/02/13	View Notes

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