773772001: Rare non-syndromic intellectual disability (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Mental state, behaviour and/or psychosocial function finding\Behaviour finding\Intellectual disability\Rare non-syndromic intellectual disability
• \Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Rare non-syndromic intellectual disability
• \Functional finding\Cognitive function finding\Intellectual ability - finding\Intellectual disability\Rare non-syndromic intellectual disability
• \Functional finding\Intelligence finding\Intellectual ability - finding\Intellectual disability\Rare non-syndromic intellectual disability
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Rare non-syndromic intellectual disability
• \Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\Rare non-syndromic intellectual disability
• \Disease\Developmental disorder\Developmental hereditary disorder\Rare non-syndromic intellectual disability

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3726303013	Rare non-syndromic intellectual disability (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3726304019	Rare non-syndromic intellectual disability	en	Synonym	Active	Case insensitive	SNOMED CT core
3726305018	A rare hereditary neurologic disease with characteristics of early-onset cognitive impairment as a sole disability. The disease may be associated with autism, epilepsy and neuromuscular deficits.	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

Description inactivation indicator reference set

REPLACED BY association reference set

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