FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

783258000: Familial dementia Danish type (disorder)


Status: current, Primitive. Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3758314017 Familial dementia Danish type en Synonym Active Initial character case insensitive SNOMED CT core
3758315016 ADan amyloidosis en Synonym Active Case sensitive SNOMED CT core
3758316015 Familial dementia Danish type (disorder) en Fully specified name Active Initial character case insensitive 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 Case sensitive 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 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 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 true Inferred relationship Some 3
ADan amyloidosis Is a Hereditary degenerative disease of central nervous system false Inferred relationship Some
ADan amyloidosis Is a ITM2B-related amyloidosis true Inferred relationship Some
ADan amyloidosis Finding site Vascular structure within brain 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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Mental health disorder reference set

Cardiovascular finding reference set

Problem/Diagnosis reference set

Back to Start