SNOMED Clinical Terms - Functional asplenia - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Functional asplenia
Synonyms	Congenital asplenia Functional asplenia (disorder)
ID	38096003
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/38096003
CONCEPTSTATUS	0
CTV3ID	XUCtt
has_associated_morphology	Congenital absence Infarct
has_clinical_course	Courses
has_finding_site	Splenic structure Structure of digestive system
has_severity	Severities
isa	Traumatic AND/OR non-traumatic injury Congenital absence of spleen Congenital anomaly of digestive system
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Disease or Syndrome Congenital Abnormality
SNOMEDID	DC-80140
SYNONYM FN	Functional asplenia (disorder)
SYNONYM IS	Congenital asplenia
TUI	T047 T019
UMLS_CUI	C0272405 C0600031

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/OMIM/MTHU016583	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0600031	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU009130	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0600031	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q89.01	ICD10CM	NLM UMLS (CUI)	CUI: C0600031	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU016583	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MDR/10053622	MedDRA	NLM UMLS (CUI)	CUI: C0600031	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU011729	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0600031	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/XE1Mi	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0600031	skos:closeMatch	loom	04/02/13	View Notes

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