FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

722980006: Dementia due to chromosomal anomaly (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3334075013 Dementia due to chromosomal anomaly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334076014 Dementia due to chromosomal anomaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334075013 Dementia due to chromosomal anomaly (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334075013 Dementia due to chromosomal anomaly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3334076014 Dementia due to chromosomal anomaly en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3334076014 Dementia due to chromosomal anomaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5835941000241117 démence due à une anomalie chromosomique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5835941000241117 démence due à une anomalie chromosomique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


6 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Dementia due to chromosomal anomaly (disorder) Due to Chromosomal disorder (disorder) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Dementia due to chromosomal anomaly (disorder) Is a Dementia associated with another disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to chromosomal anomaly (disorder) Finding site Brain structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Dementia due to chromosomal anomaly (disorder) Interprets Cognitive functions true Inferred relationship Existential restriction modifier (core metadata concept) 1
Dementia due to chromosomal anomaly (disorder) Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Dementia co-occurrent and due to Down syndrome (disorder) Is a True Dementia due to chromosomal anomaly (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Dementia due to fragile X syndrome (disorder) Is a True Dementia due to chromosomal anomaly (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Frontotemporal dementia due to TARDBP mutation Is a True Dementia due to chromosomal anomaly (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Frontotemporal dementia due to VCP mutation (disorder) Is a True Dementia due to chromosomal anomaly (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Frontotemporal dementia due to C9orf72 mutation (disorder) Is a True Dementia due to chromosomal anomaly (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Frontotemporal dementia due to FUS mutation Is a True Dementia due to chromosomal anomaly (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

Back to Start