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1259476008: Dementia due to genetic disease (disorder)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5157116018 Dementia due to genetic disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5159327016 Dementia due to genetic disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5157116018 Dementia due to genetic disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5159327016 Dementia due to genetic disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

10 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dementia due to genetic disease (disorder) Is a Dementia associated with another disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to genetic disease (disorder) Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Dementia due to genetic disease (disorder) Interprets Cognitive functions true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dementia due to genetic disease (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dementia due to genetic disease (disorder) Due to Genetic disease true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group
Dementia due to fatal familial insomnia (disorder) Is a True Dementia due to genetic disease (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to atypical pantothenate kinase associated neurodegeneration (disorder) Is a True Dementia due to genetic disease (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to classical pantothenate kinase associated neurodegeneration Is a True Dementia due to genetic disease (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to Huntington chorea Is a True Dementia due to genetic disease (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to familial Creutzfeldt-Jakob disease Is a True Dementia due to genetic disease (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to Wilson disease (disorder) Is a True Dementia due to genetic disease (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to Gerstmann Straussler Scheinker syndrome (disorder) Is a True Dementia due to genetic disease (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to fragile X syndrome (disorder) Is a True Dementia due to genetic disease (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to Rett's syndrome Is a True Dementia due to genetic disease (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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