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783618006: Lower motor neuron syndrome with late-adult onset (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
3759523010 Lower motor neuron syndrome with late-adult onset (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3759524016 Lower motor neuron syndrome with late-adult onset en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3759525015 A rare genetic motor neuron disease with characteristics of slowly progressive predominantly proximal muscular weakness and atrophy which typically manifests with muscle cramps, fasciculations, decreased/absent deep tendon reflexes, hand tremor and elevated serum creatine kinase at onset and later associates gait disturbances and impaired vibration sensation. There is evidence the disease is caused by heterozygous mutation in the CHCHD10 gene on chromosome 22q11. 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
Lower motor neuron syndrome with late-adult onset (disorder) est un(e) (attribut) atrophie musculaire spinale (trouble) true Inferred relationship Some
Lower motor neuron syndrome with late-adult onset (disorder) est un(e) (attribut) Autosomal dominant hereditary disorder true Inferred relationship Some
Lower motor neuron syndrome with late-adult onset (disorder) localisation d'une constatation (attribut) système nerveux true Inferred relationship Some 1
Lower motor neuron syndrome with late-adult onset (disorder) survenue (attribut) Adulthood (qualifier value) true Inferred relationship Some 1
Lower motor neuron syndrome with late-adult onset (disorder) est un(e) (attribut) trouble neurologique chronique true Inferred relationship Some
Lower motor neuron syndrome with late-adult onset (disorder) évolution clinique (attribut) progressif true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Canada English language reference set (foundation metadata concept)

GB English

US English

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