1156796002: Autosomal dominant cerebellar ataxia type 2 (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of brain\Disorder of brain (disorder)\Cerebellar disorder\Cerebellar ataxia\Autosomal dominant cerebellar ataxia type 2
\Head finding (finding)\Disorder of head (disorder)\Disorder of brain (disorder)\Cerebellar disorder\Cerebellar ataxia\Autosomal dominant cerebellar ataxia type 2

\Finding related to coordination / incoordination (finding)\Ataxia\...

\Hereditary ataxia (disorder)\Autosomal dominant cerebellar ataxia type 2

\Cerebellar ataxia\Autosomal dominant cerebellar ataxia type 2

\Central nervous system finding\Finding of brain\Disorder of brain (disorder)\Cerebellar disorder\Cerebellar ataxia\Autosomal dominant cerebellar ataxia type 2
\Central nervous system finding\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Cerebellar disorder\Cerebellar ataxia\Autosomal dominant cerebellar ataxia type 2

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia (disorder)\Autosomal dominant cerebellar ataxia type 2
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder (disorder)\Autosomal dominant cerebellar ataxia type 2
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia (disorder)\Autosomal dominant cerebellar ataxia type 2
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Hereditary disorder of nervous system\Hereditary ataxia (disorder)\Autosomal dominant cerebellar ataxia type 2
\Disease\Disorder of body system\Disorder of nervous system (disorder)\Disorder of the central nervous system (disorder)\Disorder of brain (disorder)\Cerebellar disorder\Cerebellar ataxia\Autosomal dominant cerebellar ataxia type 2
\Disease\Disorder of head (disorder)\Disorder of brain (disorder)\Cerebellar disorder\Cerebellar ataxia\Autosomal dominant cerebellar ataxia type 2

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

5788961000241117 ataxie cérébelleuse autosomique dominante de type 2 fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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 (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