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444024002: Multiple system atrophy, cerebellar variant (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2010. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2835514014 Multiple system atrophy, cerebellar variant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2838078010 Multiple system atrophy, cerebellar variant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2835514014 Multiple system atrophy, cerebellar variant (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2835514014 Multiple system atrophy, cerebellar variant (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2838078010 Multiple system atrophy, cerebellar variant en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2838078010 Multiple system atrophy, cerebellar variant en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5343341000241116 atrophie multisystémique, variante cérébelleuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5343341000241116 atrophie multisystémique, variante cérébelleuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multiple system atrophy, cerebellar variant (disorder) Is a Multiple system atrophy (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Multiple system atrophy, cerebellar variant (disorder) Finding site Autonomic nervous system structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Multiple system atrophy, cerebellar variant (disorder) Finding site Structure of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple system atrophy, cerebellar variant (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple system atrophy, cerebellar variant (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple system atrophy, cerebellar variant (disorder) Finding site Structure of central nervous system true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple system atrophy, cerebellar variant (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple system atrophy, cerebellar variant (disorder) Occurrence Adulthood true Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple system atrophy, cerebellar variant (disorder) Causative agent (attribute) Alpha-synuclein true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Ataxia due to multiple system atrophy, cerebellar variant (disorder) Due to True Multiple system atrophy, cerebellar variant (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 1

This concept is not in any reference sets

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