SNOMED Clinical Terms - Reticulate acropigmentation of Kitamura - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Reticulate acropigmentation of Kitamura
Synonyms	Kitamura's reticulate acropigmentation Reticulate acropigmentation of Kitamura (disorder)
ID	239133004
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/239133004
CONCEPTSTATUS	0
CTV3ID	X50Jy
has_associated_morphology	Hyperpigmentation Increased melanin pigmentation
has_clinical_course	Courses
has_episodicity	Episodicities
has_finding_site	Skin structure Skin structure of extremity
has_severity	Severities
isa	Lentigo Autosomal dominant hereditary disorder Disorder of extremity Hereditary disorder of the integument
ISPRIMITIVE	1
Semantic_Type	Disease or Syndrome
SNOMEDID	D0-70119
SYNONYM FN	Reticulate acropigmentation of Kitamura (disorder)
SYNONYM SY	Kitamura's reticulate acropigmentation
TUI	T047
UMLS_CUI	C0406811

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://www.orphanet.org/rdfns#pat_id_18010	Experimental Factor Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X50Jy	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0406811	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X50Jy	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MDR/10068651	MedDRA	NLM UMLS (CUI)	CUI: C0406811	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/179850	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0406811	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/179850	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_18010	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes

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