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1156796002: Autosomal dominant cerebellar ataxia type 2 (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4576206010 Autosomal dominant cerebellar ataxia type 2 en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4576207018 Autosomal dominant cerebellar ataxia type 2 (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
10031581000172115 ataxie cérébelleuse autosomique dominante de type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)
5021091000172119 ADCA2 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
5021101000172110 autosomaal dominante cerebellaire ataxie type 2 nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal dominant cerebellar ataxia type 2 Is a Cerebellar ataxia true Inferred relationship Some
Autosomal dominant cerebellar ataxia type 2 Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Autosomal dominant cerebellar ataxia type 2 Is a Hereditary ataxia (disorder) true Inferred relationship Some
Autosomal dominant cerebellar ataxia type 2 Finding site Cerebellar structure true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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