763186006: Grubben, De Cock, Borghgraef syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Mental state, behavior and/or psychosocial function finding\Behavior finding\Intellectual disability\Grubben, De Cock, Borghgraef syndrome
• \Functional finding\Cognitive function finding\Impaired cognition\Intellectual disability\Grubben, De Cock, Borghgraef syndrome
• \Functional finding\Cognitive function finding\Finding of intellectual ability\Intellectual disability\Grubben, De Cock, Borghgraef syndrome
• \Functional finding\Intelligence finding\Finding of intellectual ability\Intellectual disability\Grubben, De Cock, Borghgraef syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Grubben, De Cock, Borghgraef syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Grubben, De Cock, Borghgraef syndrome
• \Disease\Developmental disorder\Neurodevelopmental disorder\Intellectual disability\Grubben, De Cock, Borghgraef syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Grubben, De Cock, Borghgraef syndrome

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3638111014	Developmental delay, hypotonia, extremities hypertrophy syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3638112019	Grubben, De Cock, Borghgraef syndrome	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
3638163019	Grubben, De Cock, Borghgraef syndrome (disorder)	en	Fully specified name	Active	Entire term case sensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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