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363918005: Speech observable (observable entity)

SNOMED CT Concept\Observable entity\Clinical history/examination observable (observable entity)\Speech observable

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

487051012 Speech observable en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

770109016 Speech observable (observable entity) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

2719401000005113 træk vedr. tale da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Speech observable	Is a	Speech and language observable	false	Inferred relationship	Some
Speech observable	Is a	Clinical history/examination observable (observable entity)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Semantic dysphasia	Interprets	False	Speech observable	Inferred relationship	Some	3
Acquired dysphasia (disorder)	Interprets	False	Speech observable	Inferred relationship	Some	2
A rare hereditary ataxia characterized by recurrent episodes of ataxia with variable frequency and duration, associated with slurred speech, generalized muscle weakness and balance disturbance. Other symptoms may occur between episodes, including intention tremor, gait ataxia, mild dysarthria, myokymia, migraine and nystagmus.	Interprets	True	Speech observable	Inferred relationship	Some	1
Adult onset fluency disorder	Interprets	False	Speech observable	Inferred relationship	Some	3
Non-Alzheimer's progressive dysphasia	Interprets	True	Speech observable	Inferred relationship	Some	4
Difficulty talking	Interprets	False	Speech observable	Inferred relationship	Some	2
Ability to perform functions for speech	Is a	True	Speech observable	Inferred relationship	Some
Speech and language observable	Is a	True	Speech observable	Inferred relationship	Some
A rare genetic syndromic intellectual disability characterized by moderate to severe intellectual deficiency, language deficit (completely absent or significantly impaired speech), and distinctive facial dysmorphism (long face, straight eyebrows, and, less frequently, low-set ears and café-au-lait spots). Additional, variably observed features include motor delays, behavioral difficulties, and seizures.	Interprets	True	Speech observable	Inferred relationship	Some	2
Dysarthria	Interprets	True	Speech observable	Inferred relationship	Some	1
Spastic dysarthria	Interprets	True	Speech observable	Inferred relationship	Some	1
Flaccid dysarthria	Interprets	True	Speech observable	Inferred relationship	Some	1
Mixed dysarthria	Interprets	True	Speech observable	Inferred relationship	Some	1
Cerebellar dysarthria	Interprets	True	Speech observable	Inferred relationship	Some	1
Extrapyramidal dysarthria	Interprets	True	Speech observable	Inferred relationship	Some	1
Dysarthriapneumophonia	Interprets	True	Speech observable	Inferred relationship	Some	1
Dysarthria of velopharynx	Interprets	True	Speech observable	Inferred relationship	Some	1
Congenital dysarthria	Interprets	True	Speech observable	Inferred relationship	Some	2
Lingual dysarthria (finding)	Interprets	True	Speech observable	Inferred relationship	Some	1
Acquired dysarthria (finding)	Interprets	True	Speech observable	Inferred relationship	Some	2
A rare mitochondrial disease characterized by adult onset of the triad of sensory ataxic neuropathy, dysarthria, and ophthalmoparesis. Additional signs and symptoms are highly variable and include myopathy, seizures, and hearing loss, among others. Brain imaging may show cerebellar white matter abnormalities and/or bilateral thalamic lesions.	Interprets	True	Speech observable	Inferred relationship	Some	8
Dysarthria due to and following cerebrovascular accident (disorder)	Interprets	True	Speech observable	Inferred relationship	Some	3
Dysarthria due to and following hemorrhagic cerebrovascular accident (disorder)	Interprets	True	Speech observable	Inferred relationship	Some	3
Dysarthria due to and following ischemic cerebrovascular accident (disorder)	Interprets	True	Speech observable	Inferred relationship	Some	3
Dysarthria due to and following embolic cerebrovascular accident (disorder)	Interprets	True	Speech observable	Inferred relationship	Some	3
A rare genetic autosomal recessive spastic ataxia disease with characteristics of the onset in early childhood of spastic paraparesis, cerebellar ataxia, dysarthria and optic atrophy. Caused by homozygous mutation in the MTPAP gene on chromosome 10p11.	Interprets	True	Speech observable	Inferred relationship	Some	3
Dysarthria as late effects of cerebrovascular disease	Interprets	True	Speech observable	Inferred relationship	Some	3
Hyperkinetic dysarthria (finding)	Interprets	True	Speech observable	Inferred relationship	Some	1
Dysarthria-clumsy hand syndrome	Interprets	True	Speech observable	Inferred relationship	Some	4

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Id	Description	Lang	Type	Status	Case?	Module
487051012	Speech observable	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
770109016	Speech observable (observable entity)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2719401000005113	træk vedr. tale	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)