1365977003: Isolated childhood apraxia of speech (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Functional finding\Communication disorder\Speech and language disorder\Aphonia (disorder)\Apraxic aphonia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Functional finding\Communication disorder\Speech and language disorder\Speech and language dyspraxias\Verbal dyspraxia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Functional finding\Communication disorder\Speech and language disorder\Neurologic voice disorder\Apraxic aphonia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Functional finding\Developmental disorder of motor function\Speech and language dyspraxias\Verbal dyspraxia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Speech finding\Speech and language finding\Communication, speech and language finding\Communication disorder\Speech and language disorder\...
• \Aphonia (disorder)\Apraxic aphonia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Speech and language dyspraxias\Verbal dyspraxia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Neurologic voice disorder\Apraxic aphonia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Disease\Communication disorder\Speech and language disorder\Aphonia (disorder)\Apraxic aphonia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Disease\Communication disorder\Speech and language disorder\Speech and language dyspraxias\Verbal dyspraxia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Disease\Communication disorder\Speech and language disorder\Neurologic voice disorder\Apraxic aphonia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Disease\Developmental disorder\Neurodevelopmental disorder is a behavioral and cognitive disorder with onset during the developmental period that involves impaired or aberrant development of intellectual, motor, or social functions.\Developmental disorder of motor function\Speech and language dyspraxias\Verbal dyspraxia\Childhood apraxia of speech (disorder)\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.
• \Disease\Developmental disorder\Developmental hereditary disorder\A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-May 2025. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
5456342015	A rare neurologic disease characterized by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5456343013	A rare neurologic disease characterised by impaired ability to execute complex coordinated movements underlying the production of speech, leading to highly unintelligible speech in the absence of muscular or sensory deficits.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
5456334016	Speech-language disorder type 1	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5456335015	Isolated developmental verbal dyspraxia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5456336019	Isolated CAS (childhood apraxia of speech)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
5456337011	Isolated childhood apraxia of speech	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5456338018	Pure childhood apraxia of speech	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5456339014	Speech and language disorder with orofacial dyspraxia	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5456340011	Isolated childhood apraxia of speech (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5456341010	Pure CAS (childhood apraxia of speech)	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

Reference Sets

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

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