260379002: Impaired (qualifier value)

SNOMED CT Concept\Qualifier value\Finding value (qualifier value)\Degree findings\Impaired

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

387919014 Impaired en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

652129014 Impaired (qualifier value) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Impaired	Is a	Degree findings	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	3
SET domain containing 2, histone lysine methyltransferase-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	2
SET domain containing 2, histone lysine methyltransferase-related microcephaly, severe intellectual disability, multiple congenital anomalies syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	3
Neurexin 1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Neurexin 1-related severe neurodevelopmental disorder, motor stereotypies, chronic constipation, sleep-wake cycle disturbance (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Clark Baraitser syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Clark Baraitser syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	3
Congenital pontocerebellar hypoplasia type 11 (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	4
Congenital pontocerebellar hypoplasia type 11 (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	5
Congenital pontocerebellar hypoplasia type 14	Has interpretation	True	Impaired	Inferred relationship	Some	4
Congenital pontocerebellar hypoplasia type 14	Has interpretation	True	Impaired	Inferred relationship	Some	5
SMARCA2-related blepharophimosis, intellectual disability syndrome	Has interpretation	True	Impaired	Inferred relationship	Some	2
SMARCA2-related blepharophimosis, intellectual disability syndrome	Has interpretation	True	Impaired	Inferred relationship	Some	3
Frequent faecal incontinence	Has interpretation	True	Impaired	Inferred relationship	Some	1

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This concept is not in any reference sets