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770939009: ziekte van Huntington-achtig syndroom 3 (aandoening)


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

Descriptions:

Id Description Lang Type Status Case? Module
3703531018 Huntington disease-like 3 en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3703532013 Huntington disease-like 3 (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
6461341000146115 ziekte van Huntington-achtig syndroom 3 nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
6461351000146117 ziekte van Huntington-achtig syndroom 3 (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13068091000146115 HDL3 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13672691000146111 Huntington disease-like 3 nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
3703533015 A rare Huntington disease-like syndrome with characteristics of childhood-onset progressive neurologic deterioration with pyramidal and extrapyramidal abnormalities, chorea, dystonia, ataxia, gait instability, spasticity, seizures, mutism, and (on brain MRI) progressive frontal cortical atrophy and bilateral caudate atrophy. 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
Huntington disease-like 3 Clinical course Progressive (qualifier value) true Inferred relationship Some 1
Huntington disease-like 3 Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Huntington disease-like 3 Is a Hereditary disorder of nervous system true Inferred relationship Some
Huntington disease-like 3 Is a Huntington disease-like syndrome true Inferred relationship Some
Huntington disease-like 3 Is a Chronic brain syndrome true Inferred relationship Some
Huntington disease-like 3 Finding site Basal ganglion structure (body structure) true Inferred relationship Some 2
Huntington disease-like 3 Interprets Movement false Inferred relationship Some 3
Huntington disease-like 3 Has interpretation Abnormal true Inferred relationship Some 3
Huntington disease-like 3 Interprets Movement true Inferred relationship Some 4
Huntington disease-like 3 Interprets Movement observable true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Chorea due to Huntington disease-like 3 (disorder) Due to True Huntington disease-like 3 Inferred relationship Some 2

This concept is not in any reference sets

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