SNOMED Clinical Terms - Congenital microvillous atrophy | NCBO BioPortal

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Preferred Name	Congenital microvillous atrophy
Synonyms	Davidson disease Congenital microvillous atrophy (disorder)
ID	235729009
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/235729009
CONCEPTSTATUS	0
CTV3ID	X303M
has_clinical_course	Courses
has_finding_site	Small intestinal structure
has_severity	Severities
isa	Congenital disease Malabsorption syndrome Disorder of small intestine
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Disease or Syndrome
SNOMEDID	D5-4701F
SYNONYM FN	Congenital microvillous atrophy (disorder)
SYNONYM SY	Davidson disease
TUI	T047
UMLS_CUI	C0341306

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://www.orphanet.org/rdfns#pat_id_2157	Experimental Factor Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MDR/10068504	MedDRA	NLM UMLS (CUI)	CUI: C0341306	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/251850	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0341306	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MDR/10068494	MedDRA	NLM UMLS (CUI)	CUI: C0341306	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X303M	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0341306	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/C537470	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C0341306	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X303M	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes

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