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1187038009: Non-specific syndromic intellectual disability (disorder)

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
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
3427771001000114 Unspezifische syndromale Intelligenzminderung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3427771001000114 Unspezifische syndromale Intelligenzminderung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Non-specific syndromic intellectual disability Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
Non-specific syndromic intellectual disability Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Non-specific syndromic intellectual disability Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Non-specific syndromic intellectual disability Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Non-specific syndromic intellectual disability Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Non-specific syndromic intellectual disability Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 3
Non-specific syndromic intellectual disability Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group
Juberg Marsidi syndrome (disorder) Is a True Non-specific syndromic intellectual disability Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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