1187038009: Non-specific syndromic intellectual disability (disorder)

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

Status: current, Primitive. Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4669003011	Complex neurodevelopmental disorder	en	Synonym	Active	Case insensitive	SNOMED CT core
4669004017	Non-specific syndromic intellectual disability	en	Synonym	Active	Case insensitive	SNOMED CT core
4669005016	Non-specific syndromic intellectual disability (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4669006015	A rare genetic intellectual disability characterised by the association of intellectual disability with variable other anomalies in the absence of a well-characterised syndrome. Associated abnormalities may include facial dysmorphism, neurological signs and symptoms, behavioural problems, and abnormalities of various other organ systems.	en	Definition	Active	Case sensitive	SNOMED CT core
4669007012	A rare genetic intellectual disability characterized by the association of intellectual disability with variable other anomalies in the absence of a well-characterized syndrome. Associated abnormalities may include facial dysmorphism, neurological signs and symptoms, behavioral problems, and abnormalities of various other organ systems.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Clinical finding foundation reference set

Problem/Diagnosis reference set

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