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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
230731000052111 nedsatt 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

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
Congenital hereditary endothelial dystrophy and perceptive deafness syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	3
Oculootoradial syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	3
Mitochondrial myopathy, lactic acidosis, deafness syndrome	Has interpretation	True	Impaired	Inferred relationship	Some	1
Retinitis pigmentosa, intellectual disability, deafness, hypogenitalism syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	5
Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Black locks, oculocutaneous albinism, AND deafness of the sensorineural type	Has interpretation	True	Impaired	Inferred relationship	Some	4
Bosley Salih Alorainy syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	3
Caudal appendage deafness syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	5
Abruzzo Erickson syndrome	Has interpretation	True	Impaired	Inferred relationship	Some	4
Lowry Yong syndrome	Has interpretation	True	Impaired	Inferred relationship	Some	5
Deafness and intellectual disability Martin Probst type syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	3
Congenital cataract with deafness and hypogonadism syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	4
Deafness with cataract and skeletal anomaly syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	4
Deafness with epiphyseal dysplasia and short stature syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	4
Deafness craniofacial syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	3
Deafness with skeletal dysplasia and lip granuloma syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	4
Intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, keratoderma syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	3
Knuckle pads, leukonychia, sensorineural deafness, palmoplantar hyperkeratosis syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	5
Lipodystrophy, intellectual disability, deafness syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	5
Pili torti-deafness syndrome	Has interpretation	True	Impaired	Inferred relationship	Some	2
Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	4
X-linked sensorineural hearing loss	Has interpretation	True	Impaired	Inferred relationship	Some	1
Combined oxidative phosphorylation defect type 25 (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Acute kidney injury following administration of contrast media (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Postoperative urinary incontinence	Has interpretation	True	Impaired	Inferred relationship	Some	1
HtrA serine peptidase 1-related autosomal dominant cerebral small vessel disease (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Dementia caused by manganese and/or manganese compound (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Dementia due to thiamine deficiency (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Dementia due to niacin deficiency (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Dementia due to nutritional deficiency	Has interpretation	True	Impaired	Inferred relationship	Some	1
Dementia due to cobalamin deficiency	Has interpretation	True	Impaired	Inferred relationship	Some	1
Dementia due to vitamin E deficiency (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Cognitive impairment due to lead toxicity (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Chronic traumatic encephalopathy (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Integral membrane protein 2B related amyloidosis (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	3
Impaired social interaction	Has interpretation	True	Impaired	Inferred relationship	Some	2
Intellectual disability, epilepsy, extrapyramidal syndrome	Has interpretation	True	Impaired	Inferred relationship	Some	4
Intellectual functioning disability with aggressive behavior (finding)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Motor disability	Has interpretation	True	Impaired	Inferred relationship	Some	1
Acquired impaired spermatogenesis due to hypogonadotropic hypogonadism (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
beteendemässiga och psykiska symtom vid demens (BPSD)	Has interpretation	False	Impaired	Inferred relationship	Some	1
Moderate to severe Alzheimer's disease (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Mild dementia (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Severe dementia (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Moderate to severe Alzheimer's disease with aggressive behavior (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Renal failure requiring renal dialysis (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Huntington's chorea with hyperactive behavior (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Exacerbated heart failure	Has interpretation	True	Impaired	Inferred relationship	Some	3
New onset of heart failure	Has interpretation	True	Impaired	Inferred relationship	Some	3
Status of heart failure unchanged	Has interpretation	True	Impaired	Inferred relationship	Some	3
Severe heart failure (disorder)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Urinary incontinence in neurogenic overactive bladder (finding)	Has interpretation	True	Impaired	Inferred relationship	Some	1
Urge incontinence of urine due to bladder irritability (finding)	Has interpretation	False	Impaired	Inferred relationship	Some	2
Moderate to severe genuine stress incontinence (finding)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Heart failure following chemotherapy	Has interpretation	True	Impaired	Inferred relationship	Some	2
Fecal incontinence associated with diarrhea (finding)	Has interpretation	True	Impaired	Inferred relationship	Some	2
Urge incontinence of urine due to bladder irritability (finding)	Has interpretation	True	Impaired	Inferred relationship	Some	1

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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
230731000052111	nedsatt	sv	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Sweden NRC maintained module (core metadata concept)