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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
Dementia due to systemic lupus erythematosus Has interpretation True Impaired Inferred relationship Some 1
Dementia due to subacute sclerosing panencephalitis Has interpretation True Impaired Inferred relationship Some 1
Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome Has interpretation True Impaired Inferred relationship Some 2
Spastic paraplegia, intellectual disability, nystagmus, obesity syndrome Has interpretation True Impaired Inferred relationship Some 3
Dementia due to kuru Has interpretation True Impaired Inferred relationship Some 1
Dementia due to hemorrhagic cerebral infarction due to hypertension (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to iatrogenic Creutzfeldt-Jakob disease (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to cerebral amyloid angiopathy (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to metastatic malignant neoplasm to brain (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to Lyme disease (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to leukodystrophy Has interpretation True Impaired Inferred relationship Some 1
Dementia due to fatal familial insomnia (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to genetic disease (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to familial Creutzfeldt-Jakob disease (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to cerebral vasculitis (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to hepatic failure Has interpretation True Impaired Inferred relationship Some 1
Dementia due to hypercalcemia (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to Gerstmann Straussler Scheinker syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to fragile X syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 1
Dementia due to Hashimoto encephalopathy (disorder) Has interpretation True Impaired Inferred relationship Some 1
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Has interpretation True Impaired Inferred relationship Some 3
Megalencephaly, severe kyphoscoliosis, overgrowth syndrome Has interpretation True Impaired Inferred relationship Some 4
GRIN2B-related developmental delay, intellectual disability, autism spectrum disorder Has interpretation True Impaired Inferred relationship Some 1
GRIN2B-related developmental delay, intellectual disability, autism spectrum disorder Has interpretation True Impaired Inferred relationship Some 2
Infantile multisystem neurologic, endocrine, pancreatic disease (disorder) Has interpretation True Impaired Inferred relationship Some 5
Infantile multisystem neurologic, endocrine, pancreatic disease (disorder) Has interpretation True Impaired Inferred relationship Some 6
Frontal variant non-amnestic Alzheimer disease (disorder) Has interpretation True Impaired Inferred relationship Some 2
Logopenic non-amnestic Alzheimer disease (disorder) Has interpretation True Impaired Inferred relationship Some 2
Renal tubular necrosis following ectopic pregnancy (disorder) Has interpretation True Impaired Inferred relationship Some 2
Renal tubular necrosis following molar pregnancy (disorder) Has interpretation True Impaired Inferred relationship Some 2
Acute renal failure following ectopic pregnancy (disorder) Has interpretation True Impaired Inferred relationship Some 2
Acute renal failure following molar pregnancy (disorder) Has interpretation True Impaired Inferred relationship Some 2
Acute right ventricular failure following incision of heart (disorder) Has interpretation True Impaired Inferred relationship Some 1
Renal failure due to and following incomplete miscarriage Has interpretation True Impaired Inferred relationship Some 5
Quadrantanopia Has interpretation True Impaired Inferred relationship Some 2
Binasal heteronymous quadrantanopia (finding) Has interpretation True Impaired Inferred relationship Some 2
Bitemporal heteronymous quadrantanopia (finding) Has interpretation True Impaired Inferred relationship Some 2
Homonymous quadrant anopia Has interpretation True Impaired Inferred relationship Some 2
Left homonymous inferior quadrantanopia Has interpretation True Impaired Inferred relationship Some 2
Right homonymous superior quadrantanopia (finding) Has interpretation True Impaired Inferred relationship Some 2
Left homonymous superior quadrantanopia Has interpretation True Impaired Inferred relationship Some 2
Right homonymous inferior quadrantanopia Has interpretation True Impaired Inferred relationship Some 2
Quadrantanopia of left eye (finding) Has interpretation True Impaired Inferred relationship Some 2
Quadrantanopia of right eye (finding) Has interpretation True Impaired Inferred relationship Some 2
Peripheral visual field defect of bilateral eyes (finding) Has interpretation True Impaired Inferred relationship Some 1
Peripheral visual field defect of left eye (finding) Has interpretation True Impaired Inferred relationship Some 1
Peripheral visual field defect of right eye (finding) Has interpretation True Impaired Inferred relationship Some 1
Recurrent stress incontinence (finding) Has interpretation True Impaired Inferred relationship Some 1
Craniosynostosis, microretrognathia, severe intellectual disability syndrome Has interpretation True Impaired Inferred relationship Some 3
Craniosynostosis, microretrognathia, severe intellectual disability syndrome Has interpretation True Impaired Inferred relationship Some 4
Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency (disorder) Has interpretation True Impaired Inferred relationship Some 1
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Has interpretation True Impaired Inferred relationship Some 5
Spondylometaphyseal dysplasia, corneal dystrophy syndrome Has interpretation True Impaired Inferred relationship Some 6
Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome Has interpretation True Impaired Inferred relationship Some 3
Posterior-predominant lissencephaly, broad flat pons and medulla-midline crossing defects syndrome Has interpretation True Impaired Inferred relationship Some 4
Primary hypomagnesemia, refractory seizures, intellectual disability syndrome Has interpretation True Impaired Inferred relationship Some 2
Primary hypomagnesemia, refractory seizures, intellectual disability syndrome Has interpretation True Impaired Inferred relationship Some 3
Infection-related hemolytic uremic syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 1
Visual field defect due to and following intracerebral haemorrhage Has interpretation True Impaired Inferred relationship Some 4
Urinary incontinence due to and following cerebrovascular accident (disorder) Has interpretation True Impaired Inferred relationship Some 1
Urinary incontinence due to and following cerebrovascular accident with intracranial hemorrhage (disorder) Has interpretation True Impaired Inferred relationship Some 1
Urinary incontinence due to and following embolic cerebrovascular accident (disorder) Has interpretation True Impaired Inferred relationship Some 1
Combined oxidative phosphorylation defect type 39 Has interpretation True Impaired Inferred relationship Some 1
Combined oxidative phosphorylation defect type 39 Has interpretation True Impaired Inferred relationship Some 2
Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome Has interpretation True Impaired Inferred relationship Some 7
Short stature, skeletal dysplasia, retinal degeneration, intellectual disability, sensorineural hearing loss syndrome Has interpretation True Impaired Inferred relationship Some 8
Frontotemporal dementia Has interpretation True Impaired Inferred relationship Some 3
Pick's disease with Pick bodies Has interpretation True Impaired Inferred relationship Some 3
Pick's disease with Pick cells and no Pick bodies Has interpretation True Impaired Inferred relationship Some 3
Frontal lobe degeneration with motor neurone disease Has interpretation True Impaired Inferred relationship Some 3
Semantic dementia Has interpretation True Impaired Inferred relationship Some 4
Frontotemporal dementia with gene located on 3p11 (disorder) Has interpretation True Impaired Inferred relationship Some 3
Right temporal atrophy variant frontotemporal dementia (disorder) Has interpretation True Impaired Inferred relationship Some 1
Behavioral variant of frontotemporal dementia (disorder) Has interpretation True Impaired Inferred relationship Some 3
Altered behavior due to Pick's disease (disorder) Has interpretation True Impaired Inferred relationship Some 5
Frontotemporal dementia due to TARDBP mutation Has interpretation True Impaired Inferred relationship Some 4
Frontotemporal dementia due to VCP mutation (disorder) Has interpretation True Impaired Inferred relationship Some 4
Frontotemporal dementia due to C9orf72 mutation (disorder) Has interpretation True Impaired Inferred relationship Some 4
Frontotemporal dementia due to FUS mutation Has interpretation True Impaired Inferred relationship Some 4
Amyotrophic lateral sclerosis with frontotemporal dementia (disorder) Has interpretation True Impaired Inferred relationship Some 3
Hepatorenal syndrome with acute kidney injury (disorder) Has interpretation True Impaired Inferred relationship Some 1
Pornographomania Has interpretation True Impaired Inferred relationship Some 1
Tricuspid valve stenosis with regurgitation due to neuroendocrine tumor (disorder) Has interpretation True Impaired Inferred relationship Some 2
Tricuspid valve regurgitation due to neuroendocrine tumor (disorder) Has interpretation True Impaired Inferred relationship Some 2
Post-renal acute kidney injury Has interpretation True Impaired Inferred relationship Some 1
Intra-renal acute kidney injury (disorder) Has interpretation True Impaired Inferred relationship Some 1
Atypical haemolytic uraemic syndrome with complement gene abnormality Has interpretation True Impaired Inferred relationship Some 2
Atypical haemolytic uraemic syndrome with anti-factor H antibodies Has interpretation True Impaired Inferred relationship Some 2
Osteoporosis due to chronic kidney disease (disorder) Has interpretation True Impaired Inferred relationship Some 5
Aldehyde dehydrogenase 18 family member A1-related de Barsy syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 5
Aldehyde dehydrogenase 18 family member A1-related de Barsy syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 6
Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome Has interpretation True Impaired Inferred relationship Some 5
Pyrroline-5-carboxylate reductase 1 related de Barsy syndrome Has interpretation True Impaired Inferred relationship Some 6
Cystic fibrosis due to heterozygous deltaF508 mutation Has interpretation True Impaired Inferred relationship Some 1
Cystic fibrosis due to homozygous deltaF508 mutation Has interpretation True Impaired Inferred relationship Some 1
Acute exacerbation of chronic heart failure Has interpretation True Impaired Inferred relationship Some 1
Nasal step visual field defect of right eye (finding) Has interpretation True Impaired Inferred relationship Some 1
Nasal step visual field defect of left eye (finding) Has interpretation True Impaired Inferred relationship Some 1
Nasal step visual field defect of bilateral eyes (finding) Has interpretation True Impaired Inferred relationship Some 1
Adipsic arginine vasopressin-related polyuria (disorder) Has interpretation True Impaired Inferred relationship Some 1
Cyclin dependent kinase 13-related congenital heart defects, intellectual disability, facial dysmorphism syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 2

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