SNOMED Clinical Terms - Gastroschisis - Terms

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Preferred Name	Gastroschisis
Synonyms	Gastroschisis (disorder)
ID	72951007
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/72951007
CONCEPTSTATUS	0
CTV3ID	PG71.
has_associated_morphology	Congenital protrusion Hernial opening Congenital failure of fusion Hernia
has_clinical_course	Courses
has_finding_site	Intestinal structure Abdominal wall structure
has_severity	Severities
isa	Congenital malformation Hernia of abdominal wall Intestinal hernia Congenital anomaly of abdominal wall Congenital anomaly of intestinal tract
ISPRIMITIVE	1
occurs_in	Congenital
Semantic_Type	Congenital Abnormality Disease or Syndrome
SNOMEDID	D4-16611
SYNONYM FN	Gastroschisis (disorder)
TUI	T019 T047
UMLS_CUI	C0265706

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.org/obo/owl/HP#HP_0001543	Bone Dysplasia Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.semanticweb.org/ontologies/2012/11/abnormalities.owl#phenodb:1015	Fanconi Anemia (FA) Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD9CM/756.73	International Classification of Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q79.3	ICD10CM	NLM UMLS (CUI)	CUI: C0265706	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/230750	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MDR/10018046	MedDRA	NLM UMLS (CUI)	CUI: C0265706	skos:closeMatch	loom	04/02/13	View Notes
http://purl.obolibrary.org/obo/DOID_11044	NIF Dysfunction	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MDR/10018046	MedDRA	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.owl-ontologies.com/NPOntology.owl#DOID_11044	Natural Products Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#sgn_id_17330	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.obolibrary.org/obo/HP_0001543	Human Phenotype Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/PG71.	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0265706	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/NDFRT/N0000003997	National Drug File	NLM UMLS (CUI)	CUI: C0265706	skos:closeMatch	loom	04/02/13	View Notes
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Gastroschisis	NCI Thesaurus	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU009129	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0265706	skos:closeMatch	loom	04/02/13	View Notes
http://purl.obolibrary.org/obo/DOID_11044	Neuroscience Information Framework Standard ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/CST/ANOMALY%20CONGEN	Coding Symbols for a Thesaurus of Adverse Reaction Terms	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://bioonto.de/mesh.owl#C16.131.621.417	OWL Version of MeSH	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_731	Experimental Factor Ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/CST/ANOMALY%20CONGEN	Coding Symbols for a Thesaurus of Adverse Reaction Terms	NLM UMLS (CUI)	CUI: C0265706	skos:closeMatch	loom	04/02/13	View Notes
http://bioonto.de/mesh.owl#D020139	OWL Version of MeSH	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU009129	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://bioonto.de/mesh.owl#C05.660.417	OWL Version of MeSH	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/RCD/PG71.	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://www.orphanet.org/rdfns#pat_id_731	Orphanet Ontology of Rare Diseases	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/NDFRT/N0000003997	National Drug File	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q79.3	ICD10CM	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD9CM/756.73	International Classification of Diseases	NLM UMLS (CUI)	CUI: C0265706	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10/Q79.3	ICD10	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://bioonto.de/mesh.owl#C23.300.707.374.500	OWL Version of MeSH	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://uwhealth.org/himc/icd/icd09/#756.73	ICD09	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/OMIM/230750	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0265706	skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/D020139	Medical Subject Headings (MeSH)	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.obolibrary.org/obo/DOID_11044	Human disease ontology	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/ICD10/Q79.3	ICD10	NLM UMLS (CUI)	CUI: C0265706	skos:closeMatch	loom	04/02/13	View Notes
http://purl.obolibrary.org/obo/MP_0000757	Mammalian phenotype	NCBO (lexical mapping)		skos:closeMatch	loom	04/02/13	View Notes
http://purl.bioontology.org/ontology/MSH/D020139	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C0265706	skos:closeMatch	loom	04/02/13	View Notes

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