SNOMED Clinical Terms - Aplasia cutis congenita - Terms | NCBO BioPortal

SNOMED Clinical Terms Summary

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Preferred Name	Aplasia cutis congenita
Synonyms	Epitheliogenesis imperfecta Congenital absence of skin ACC - Aplasia cutis congenita Cutis aplasia Aplasia cutis congenita (disorder)
ID	35484002
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/35484002
CONCEPTSTATUS	0
CTV3ID	X78Dv
has_associated_morphology	Congenital absence
has_clinical_course	Courses
has_finding_site	Skin structure
has_severity	Severities
isa	Congenital malformation Congenital anomaly of skin Aplasia of skin
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Congenital Abnormality
SNOMEDID	D4-40120
SYNONYM FN	Aplasia cutis congenita (disorder)
SYNONYM SY	Epitheliogenesis imperfecta Congenital absence of skin ACC - Aplasia cutis congenita Cutis aplasia
TUI	T019
UMLS_CUI	C0282160

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/MSH/D004476	Medical Subject Headings (MeSH)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/D004476	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C0282160	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X78Du	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0282160	skos:closeMatch	loom	04/02/13	View Notes
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:2111	Fanconi Anemia (FA) Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/107600	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0282160	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU020179	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MDR/10002963	MedDRA	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Aplasia_Cutis_Congenita	NCI Thesaurus	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU019222	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0282160	skos:closeMatch	loom	04/02/13	View Notes
http://purl.org/obo/owl/HP#HP_0001057	Bone Dysplasia Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:0106	Fanconi Anemia (FA) Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MDR/10002963	MedDRA	NLM UMLS (CUI)	CUI: C0282160	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X78Dv	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/X78Dv	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0282160	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q84.8	ICD10CM	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU020179	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0282160	skos:closeMatch	loom	04/02/13	View Notes
http://purl.obolibrary.org/obo/HP_0001057	Human Phenotype Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q84.8	ICD10CM	NLM UMLS (CUI)	CUI: C0282160	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU019222	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes

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