SNOMED Clinical Terms - Congenital factor IX deficiency variant - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Congenital factor IX deficiency variant
Synonyms	Congenital factor IX deficiency variant (disorder)
ID	234444001
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/234444001
CONCEPTSTATUS	0
CTV3ID	X20EI
has_clinical_course	Courses
has_severity	Severities
isa	Hereditary factor IX deficiency disease Congenital disease
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Disease or Syndrome
SNOMEDID	DC-63161
SYNONYM FN	Congenital factor IX deficiency variant (disorder)
TUI	T047
UMLS_CUI	C0398607

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/RCD/X20EI	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0398607	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X20EI	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes

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