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783258000: ADan-amyloïdose (aandoening)

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
9385941000146115 familiaire dementie Deens type nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
9385961000146119 familiaire vorm van dementie Deens type nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10537811000146110 ADan-amyloïdose nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
10923271000146116 ADan-amyloïdose (aandoening) nl Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
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

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

This concept is not in any reference sets

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