230787005: Congenital expressive dysphasia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Central nervous system finding\Finding of brain\Encephalopathy\Congenital dysphasia\Congenital expressive dysphasia
• \Central nervous system finding\Disorder of the central nervous system\Encephalopathy\Congenital dysphasia\Congenital expressive dysphasia
• \Finding of head and neck region\Head finding\...
• \Finding of brain\Encephalopathy\Congenital dysphasia\Congenital expressive dysphasia
• \Disorder of head\Encephalopathy\Congenital dysphasia\Congenital expressive dysphasia
• \Speech finding\Speech impairment\Dysphasia\Congenital dysphasia\Congenital expressive dysphasia
• \Neurological finding\Aphasia, agnosia, dyslexia AND/OR apraxia\Dyslexia AND/OR speech dysfunction\Dysphasia\Congenital dysphasia\Congenital expressive dysphasia
• \Disease\Disorder of body system\Neurological disorder\Disorder of the central nervous system\Encephalopathy\Congenital dysphasia\Congenital expressive dysphasia
• \Disease\Disorder of head\Encephalopathy\Congenital dysphasia\Congenital expressive dysphasia
• \Disease\Congenital disease\Congenital dysphasia\Congenital expressive dysphasia

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
345788016	Congenital expressive dysphasia	en	Synonym	Active	Case insensitive	SNOMED CT core
618641012	Congenital expressive dysphasia (disorder)	en	Fully specified name	Active	Case insensitive	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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