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253185002: Chiari malformation type I (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
377081010 Chiari malformation type I en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
643914014 Chiari malformation type I (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
2966580013 Arnold Chiari type 1 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1860931000195113 malformazione di Chiari tipo I it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
209771000172117 malformation de Chiari de type 1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
551831000172111 malformation d'Arnold-Chiari de type 1 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429331001000117 Arnold-Chiari-Fehlbildung Typ I de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chiari malformation type I Is a Chiari malformation (disorder) true Inferred relationship Some
Chiari malformation type I Finding site Brain tissue structure false Inferred relationship Some 1
Chiari malformation type I Occurrence Congenital false Inferred relationship Some
Chiari malformation type I Associated morphology anomalie congénitale false Inferred relationship Some 1
Chiari malformation type I Associated morphology Congenital protrusion false Inferred relationship Some 1
Chiari malformation type I Associated morphology Herniated structure (morphologic abnormality) false Inferred relationship Some 1
Chiari malformation type I Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Some 1
Chiari malformation type I Associated morphology Congenital protrusion false Inferred relationship Some 1
Chiari malformation type I Finding site Brain tissue structure false Inferred relationship Some 1
Chiari malformation type I Occurrence Congenital false Inferred relationship Some 2
Chiari malformation type I Associated morphology Congenital protrusion false Inferred relationship Some 2
Chiari malformation type I Finding site Brain tissue structure false Inferred relationship Some 2
Chiari malformation type I Occurrence Congenital true Inferred relationship Some 1
Chiari malformation type I Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Chiari malformation type I Finding site Cerebellar structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
A rare syndromic craniosynostosis characterized by sagittal craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis. Other clinical findings include blepharophimosis, small low-set ears, hypoplastic philtrum, kidney malformation, and hypogenitalism. Is a True Chiari malformation type I Inferred relationship Some

Reference Sets

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