260379002: gestoord (kwalificatiewaarde)

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:

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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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
4541301000146114	gestoord	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4541311000146111	gestoord (kwalificatiewaarde)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4541321000146118	beperkt	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4541331000146116	gebrekkig	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
4541341000146112	verstoord	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)