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770939009: Huntington disease-like 3 (disorder)


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
5404965014 Huntington disease-like 3 is a rare Huntington disease-like syndrome characterized by 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
5404966010 Huntington disease-like 3 is a rare Huntington disease-like syndrome characterised by 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
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
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
5404965014 Huntington disease-like 3 is a rare Huntington disease-like syndrome characterized by 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
5404966010 Huntington disease-like 3 is a rare Huntington disease-like syndrome characterised by 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
3421681001000112 Chorea Huntington-ähnliche Krankheit 3 de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
882121000172115 maladie de Huntington-like 3 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
964801000172116 HDL3 - Huntington disease-like 3 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
882121000172115 maladie de Huntington-like 3 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
964801000172116 HDL3 - Huntington disease-like 3 fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3421681001000112 Chorea Huntington-ähnliche Krankheit 3 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
Huntington disease-like 3 Clinical course Progressive true Inferred relationship Existential restriction modifier (core metadata concept) 1
Huntington disease-like 3 Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Huntington disease-like 3 Is a Hereditary disorder of nervous system (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Huntington disease-like 3 Is a Huntington disease-like syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Huntington disease-like 3 Is a Chronic brain syndrome (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Huntington disease-like 3 Finding site Basal ganglion structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Huntington disease-like 3 Interprets Movement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Huntington disease-like 3 Has interpretation Abnormal true Inferred relationship Existential restriction modifier (core metadata concept) 3
Huntington disease-like 3 Interprets Movement true Inferred relationship Existential restriction modifier (core metadata concept) 4
Huntington disease-like 3 Interprets Movement observable true Inferred relationship Existential restriction modifier (core metadata concept) 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 Existential restriction modifier (core metadata concept) 2

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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