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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
4240381000005114 Chiaris misdannelse type I da Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Danish module (core metadata concept)


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Chiari malformation type I Is a Chiari malformation 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 kongenit anomali false Inferred relationship Some 1
Chiari malformation type I Associated morphology kongenit 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 kongenit 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 kongenit 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

Description inactivation indicator reference set

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