Preferred Name

Chiari malformation
Synonyms

Chiari malformation (disorder)

Arnold-Chiari syndrome
ID

253184003
Full Id

http://purl.bioontology.org/ontology/SNOMEDCT/253184003
associated_with

Closed spina bifida with Arnold-Chiari malformation
CONCEPTSTATUS

0
CTV3ID

X77rk
has_associated_morphology

Congenital protrusion
has_clinical_course

Courses
has_finding_site

Brain tissue structure
has_severity

Severities
inverse_may_be_a

(Spina bifida + hydrocephalus) or (Arnold-Chiari syndrome)

(Spina bifida with hydrocephalus) or (Arnold-Chiari syndrome)

(Spina bifida + hydrocephalus) or (Arnold-Chiari syndrome)

Arnold-Chiari syndrome

(Arnold-Chiari syndrome) or (closed spina bifida with Arnold-Chiari malformation)
isa

Congenital malformation

Congenital anomaly of brain
ISPRIMITIVE

1
occurs_in

Congenital
Semantic_Type

Congenital Abnormality
SNOMEDID

D4-90061
SYNONYM FN

Chiari malformation (disorder)
SYNONYM SY

Arnold-Chiari syndrome
TUI

T019
UMLS_CUI

C0003803
Create New Mapping

Mapping To Ontology Source Comment Relationship Added By Added On Notes
http://purl.bioontology.org/ontology/ICD10CM/Q07.0 ICD10CM NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MSH/D001139 Medical Subject Headings (MeSH) NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes
http://bioontology.org/projects/ontologies/radlex/radlexOwlDlComponent#RID28827 RadLex NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/ICD10/Q07.0 ICD10 NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU010483 Online Mendelian Inheritance in Man NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/NDFRT/N0000000467 National Drug File NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/XE1Ja Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/X77rk Read Codes, Clinical Terms Version 3 (CTV3) NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/ICD10CM/Q07.0 ICD10CM NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/RCD/X77rk Read Codes, Clinical Terms Version 3 (CTV3) NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU010483 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10008503 MedDRA NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MEDLINEPLUS/T3022 MedlinePlus Health Topics NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes
http://purl.obolibrary.org/obo/HP_0002308 Human Phenotype Ontology NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/ICD10/Q07.0 ICD10 NCBO (lexical mapping) skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10008503 MedDRA NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/MDR/10003101 MedDRA NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes
http://purl.bioontology.org/ontology/OMIM/MTHU007642 Online Mendelian Inheritance in Man NLM UMLS (CUI) CUI: C0003803 skos:closeMatch loom 04/02/13 View Notes

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