SNOMED Clinical Terms - Congenital color blindness | NCBO BioPortal

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Preferred Name	Congenital color blindness
Synonyms	Congenital colour blindness Congenital color blindness (disorder)
ID	232148006
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/232148006
CONCEPTSTATUS	0
CTV3ID	X00gL
has_clinical_course	Courses
has_finding_site	Retinal structure
has_severity	Severities
isa	Color blindness Congenital disease Color vision deficiency
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Congenital Abnormality
SNOMEDID	DA-74406
SYNONYM FN	Congenital color blindness (disorder)
SYNONYM PTGB	Congenital colour blindness
TUI	T019
UMLS_CUI	C0339697

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/RCD/X00gL	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X00gL	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0339697	skos:closeMatch	loom	04/02/13	View Notes

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