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1186856001: Atypical pantothenate kinase associated neurodegeneration (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4667845016 Atypical pantothenate kinase associated neurodegeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4667846015 Atypical pantothenate kinase associated neurodegeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4667845016 Atypical pantothenate kinase associated neurodegeneration (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4667846015 Atypical pantothenate kinase associated neurodegeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5808061000241115 neurodégénérescence atypique associée à la pantothénate kinase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5808061000241115 neurodégénérescence atypique associée à la pantothénate kinase 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
Atypical pantothenate kinase associated neurodegeneration (disorder) Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier (core metadata concept)
Atypical pantothenate kinase associated neurodegeneration (disorder) Is a Pigmentary pallidal degeneration true Inferred relationship Existential restriction modifier (core metadata concept)
Atypical pantothenate kinase associated neurodegeneration (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Atypical pantothenate kinase associated neurodegeneration (disorder) Interprets Movement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Atypical pantothenate kinase associated neurodegeneration (disorder) Finding site Globus pallidus structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Atypical pantothenate kinase associated neurodegeneration (disorder) Associated morphology Pigmentary degeneration true Inferred relationship Existential restriction modifier (core metadata concept) 1
Atypical pantothenate kinase associated neurodegeneration (disorder) Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 2
Atypical pantothenate kinase associated neurodegeneration (disorder) Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 3
Atypical pantothenate kinase associated neurodegeneration (disorder) Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group
Dementia due to atypical pantothenate kinase associated neurodegeneration (disorder) Due to True Atypical pantothenate kinase associated neurodegeneration (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 3
Dystonia due to atypical pantothenate kinase associated neurodegeneration (disorder) Due to True Atypical pantothenate kinase associated neurodegeneration (disorder) Inferred relationship Existential restriction modifier (core metadata concept) 3

This concept is not in any reference sets

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