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260379002: Impaired (qualifier value)

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

0 descendants.

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
Temporary auditory threshold shift of left ear (disorder) Has interpretation True Impaired Inferred relationship Some 2
Right temporary auditory threshold shift Has interpretation True Impaired Inferred relationship Some 2
Frequent faecal incontinence Has interpretation True Impaired Inferred relationship Some 1
Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome Has interpretation True Impaired Inferred relationship Some 2
Infantile neurodegeneration, progressive spasticity, intellectual disability, white matter lesions syndrome Has interpretation True Impaired Inferred relationship Some 3
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome Has interpretation True Impaired Inferred relationship Some 2
Neurodevelopmental delay, hypotonia, cerebellar ataxia, cardiac conduction defects syndrome Has interpretation True Impaired Inferred relationship Some 3
Heart failure following administration of antineoplastic agent Has interpretation True Impaired Inferred relationship Some 1
Microphthalmia with brain atrophy syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 3
Microphthalmia with brain atrophy syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 4
Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 1
Myelin transcription factor 1 like-related developmental delay, intellectual disability, obesity syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 2
Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 2
Blepharophimosis, intellectual disability syndrome/genitopatellar overlap syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 3
Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation (disorder) Has interpretation True Impaired Inferred relationship Some 2
Autosomal dominant intellectual disability, craniofacial dysmorphism, macrocephaly, hypotonia syndrome due to H1.4 linker histone, cluster member mutation (disorder) Has interpretation True Impaired Inferred relationship Some 3
Dysequilibrium syndrome Has interpretation True Impaired Inferred relationship Some 2
Dysequilibrium syndrome Has interpretation True Impaired Inferred relationship Some 3
CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome Has interpretation True Impaired Inferred relationship Some 2
CCNK-related neurodevelopmental disorder, severe intellectual disability, facial dysmorphism syndrome Has interpretation True Impaired Inferred relationship Some 3
AMeD syndrome Has interpretation True Impaired Inferred relationship Some 3
AMeD syndrome Has interpretation True Impaired Inferred relationship Some 4
Hypertension in chronic kidney disease stage 3B due to type 1 diabetes mellitus Has interpretation True Impaired Inferred relationship Some 1
Hypertension in chronic kidney disease stage 3A due to type 1 diabetes mellitus (disorder) Has interpretation True Impaired Inferred relationship Some 1
Hypertension in chronic kidney disease stage 3 due to type 1 diabetes mellitus (disorder) Has interpretation True Impaired Inferred relationship Some 1
Hypertension in chronic kidney disease stage 2 due to type 1 diabetes mellitus (disorder) Has interpretation True Impaired Inferred relationship Some 1
Hypertension in chronic kidney disease stage 3B due to type 2 diabetes mellitus (disorder) Has interpretation True Impaired Inferred relationship Some 1
Hypertension in chronic kidney disease stage 3A due to type 2 diabetes mellitus Has interpretation True Impaired Inferred relationship Some 1
Hypertension in chronic kidney disease stage 5 due to type 1 diabetes mellitus Has interpretation True Impaired Inferred relationship Some 1
Hypertension in chronic kidney disease stage 4 due to type 1 diabetes mellitus Has interpretation True Impaired Inferred relationship Some 1
Chronic kidney disease stage 3B due to type 2 diabetes mellitus (disorder) Has interpretation True Impaired Inferred relationship Some 1
Chronic kidney disease stage 3A due to type 2 diabetes mellitus Has interpretation True Impaired Inferred relationship Some 1
Chronic kidney disease stage 3B due to type 1 diabetes mellitus Has interpretation True Impaired Inferred relationship Some 1
Chronic kidney disease stage 3A due to type 1 diabetes mellitus Has interpretation True Impaired Inferred relationship Some 1
CIMDAG syndrome Has interpretation True Impaired Inferred relationship Some 4
CIMDAG syndrome Has interpretation True Impaired Inferred relationship Some 5
Chromodomain helicase DNA binding protein 4-related neurodevelopmental disorder (disorder) Has interpretation True Impaired Inferred relationship Some 2
Chromodomain helicase DNA binding protein 4-related neurodevelopmental disorder (disorder) Has interpretation True Impaired Inferred relationship Some 3
Cleft palate, congenital heart defect, intellectual disability syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 3
Cleft palate, congenital heart defect, intellectual disability syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 4
Radiation induced taste impairment Has interpretation True Impaired Inferred relationship Some 2
Dementia caused by ionizing radiation Has interpretation True Impaired Inferred relationship Some 2
Urinary incontinence due to and following ischemic cerebrovascular accident (disorder) Has interpretation True Impaired Inferred relationship Some 1
CPE-related Prader-Willi-like syndrome Has interpretation True Impaired Inferred relationship Some 4
CPE-related Prader-Willi-like syndrome Has interpretation True Impaired Inferred relationship Some 5

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