1187038009: Non-specific syndromic intellectual disability (disorder)

• SNOMED CT Concept\Clinical finding (finding)\Disease\...
• \Genetic disease\Hereditary disease\Developmental hereditary disorder\Non-specific syndromic intellectual disability
• \Mental disorder\Developmental mental disorder\Intellectual disability\Non-specific syndromic intellectual disability
• \Developmental disorder\Neurodevelopmental disorder\Developmental mental disorder\Intellectual disability\Non-specific syndromic intellectual disability
• \Developmental disorder\Developmental hereditary disorder\Non-specific syndromic intellectual disability

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
4669003011	Complex neurodevelopmental disorder	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4669004017	Non-specific syndromic intellectual disability	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4669005016	Non-specific syndromic intellectual disability (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	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	Entire term case sensitive (core metadata concept)	SNOMED CT core
5318311000052116	ospecifikt syndrom med intellektuell funktionsnedsättning	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

This concept is not in any reference sets

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