721220004: Familial developmental dysphasia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Speech finding\Speech impairment\Dysphasia\Developmental dysphasia\Familial developmental dysphasia
• \Neurological finding\Aphasia, agnosia, dyslexia AND/OR apraxia\Dyslexia AND/OR speech dysfunction\Dysphasia\Developmental dysphasia\Familial developmental dysphasia
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Familial developmental dysphasia
• \Disease\Familial disease\Familial developmental dysphasia

Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3324652014	Familial developmental dysphasia (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3324653016	Familial developmental dysphasia	en	Synonym	Active	Case insensitive	SNOMED CT core
3324654010	Billard Toutain Maheut syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3324655011	A severe form of developmental verbal apraxia with characteristics of a deficit in spontaneous speech, writing, grammatical judgment and repetition, defective articulation, moderate to severe degree of dyspraxia, a reduced use of consonant clusters and comprehension delay. Hearing and intelligence are normal. Inheritance is autosomal dominant with full penetrance.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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