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783258000: Familial dementia Danish type (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3758314017 Familial dementia Danish type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3758315016 ADan amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3758316015 Familial dementia Danish type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3758317012 A rare neurodegenerative disease with characteristics of progressive cataracts, hearing loss, cerebellar ataxia, paranoid psychosis and dementia. Neuropathological features are diffuse atrophy of all parts of the brain, chronic diffuse encephalopathy and the presence of extremely thin and almost completely demyelinated cranial nerves. Caused by mutation in the ITM2B gene. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3758314017 Familial dementia Danish type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3758315016 ADan amyloidosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3758316015 Familial dementia Danish type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3758317012 A rare neurodegenerative disease with characteristics of progressive cataracts, hearing loss, cerebellar ataxia, paranoid psychosis and dementia. Neuropathological features are diffuse atrophy of all parts of the brain, chronic diffuse encephalopathy and the presence of extremely thin and almost completely demyelinated cranial nerves. Caused by mutation in the ITM2B gene. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3429461001000115 ADan-Amyloidose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6168501000241117 amyloïdose ADan fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6168511000241115 amylose ADan fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6168521000241110 démence familiale de type danoise fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6168501000241117 amyloïdose ADan fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6168511000241115 amylose ADan fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6168521000241110 démence familiale de type danoise fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3429461001000115 ADan-Amyloidose de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
ADan amyloidosis Is a Autosomal dominant hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
ADan amyloidosis Is a Dementia false Inferred relationship Existential restriction modifier (core metadata concept)
ADan amyloidosis Is a Chronic organic mental disorder (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
ADan amyloidosis Finding site Brain structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
ADan amyloidosis Is a Hereditary disorder of nervous system (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
ADan amyloidosis Is a Hereditary amyloidosis (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
ADan amyloidosis Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
ADan amyloidosis Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier (core metadata concept) 1
ADan amyloidosis Is a Chronic metabolic disorder false Inferred relationship Existential restriction modifier (core metadata concept)
ADan amyloidosis Interprets Cognitive functions true Inferred relationship Existential restriction modifier (core metadata concept) 2
ADan amyloidosis Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 3
ADan amyloidosis Is a Hereditary degenerative disease of central nervous system false Inferred relationship Existential restriction modifier (core metadata concept)
ADan amyloidosis Is a Integral membrane protein 2B related amyloidosis (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
ADan amyloidosis Finding site Vascular structure within brain (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
ADan amyloidosis Finding site Structure of parenchyma of brain true Inferred relationship Existential restriction modifier (core metadata concept) 4
ADan amyloidosis Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier (core metadata concept) 4
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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