SNOMED Clinical Terms - Cranioschisis - Terms

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Preferred Name	Cranioschisis
Synonyms	Cranium bifidum Cranioschisis (disorder)
ID	48777005
Full Id	http://purl.bioontology.org/ontology/SNOMEDCT/48777005
CONCEPTSTATUS	0
CTV3ID	X50Kd
has_associated_morphology	Congenital failure of fusion
has_clinical_course	Courses
has_finding_site	Bone structure of cranium
has_severity	Severities
isa	Congenital malformation Congenital abnormality of skull shape
ISPRIMITIVE	0
occurs_in	Congenital
Semantic_Type	Congenital Abnormality Disease or Syndrome
SNOMEDID	D4-11230
SYNONYM FN	Cranioschisis (disorder)
SYNONYM SY	Cranium bifidum
TUI	T019 T047
UMLS_CUI	C0265541 C0014065

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Mapping To	Ontology	Source	Comment	Relationship	Added By	Added On	Notes
http://purl.bioontology.org/ontology/ICD10CM/Q01	ICD10CM	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/NDFRT/N0000001083	National Drug File	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MSH/D009421	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C0265541	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/WHO/0753	WHO Adverse Reaction Terminology	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/X50Kd	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0265541	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU002500	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/X50Kd	Read Codes, Clinical Terms Version 3 (CTV3)	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/P20z.	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/XE1Ji	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/ICD9CM/742.0	International Classification of Diseases	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/ICD10/Q01	ICD10	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/CST/ENCEPHALOCELE	Coding Symbols for a Thesaurus of Adverse Reaction Terms	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU000609	Online Mendelian Inheritance in Man	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MSH/D009421	Medical Subject Headings (MeSH)	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MDR/10014617	MedDRA	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/MSH/D004677	Medical Subject Headings (MeSH)	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/RCD/X77qE	Read Codes, Clinical Terms Version 3 (CTV3)	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.obolibrary.org/obo/MP_0000919	Mammalian phenotype	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/ICD10/Q01.9	ICD10	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU000609	Online Mendelian Inheritance in Man	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes
http://purl.org/obo/owl/MP#MP_0000919	Suggested Ontology for Pharmacogenomics	NCBO (lexical mapping)		skos:closeMatch	loom	05/21/13	View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q01.9	ICD10CM	NLM UMLS (CUI)	CUI: C0014065	skos:closeMatch	loom	05/21/13	View Notes

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