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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
119831000077116 altéré fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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
Chloride voltage-gated channel 4-related X-linked intellectual disability syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 3
X-linked female restricted facial dysmorphism, short stature, choanal atresia, intellectual disability Has interpretation True Impaired Inferred relationship Some 3
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 7
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome Has interpretation True Impaired Inferred relationship Some 8
Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome Has interpretation True Impaired Inferred relationship Some 6
Peripheral myelin protein 22-retinoic acid induced 1 contiguous gene duplication syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 5
Combined oxidative phosphorylation defect type 23 Has interpretation True Impaired Inferred relationship Some 7
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome Has interpretation True Impaired Inferred relationship Some 7
Infantile inflammatory bowel disease with neurological involvement (disorder) Has interpretation True Impaired Inferred relationship Some 5
Intellectual disability, cardiac anomalies, short stature, joint laxity syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 3
Gabriele-de Vries syndrome Has interpretation True Impaired Inferred relationship Some 3
GNB5-related intellectual disability, cardiac arrhythmia syndrome Has interpretation True Impaired Inferred relationship Some 4
Growth delay, intellectual disability, hepatopathy syndrome Has interpretation True Impaired Inferred relationship Some 4
Non-specific syndromic intellectual disability Has interpretation True Impaired Inferred relationship Some 3
STAG1-related intellectual disability, facial dysmorphism, gastrooesophageal reflux syndrome Has interpretation True Impaired Inferred relationship Some 3
Early-onset seizures, distal limb anomalies, facial dysmorphism, global developmental delay syndrome Has interpretation True Impaired Inferred relationship Some 4
Witteveen Kolk syndrome Has interpretation True Impaired Inferred relationship Some 3
Micrognathia, recurrent infections, behavioural abnormalities, mild intellectual disability syndrome Has interpretation True Impaired Inferred relationship Some 4
Microcephalic cortical malformations, short stature due to rotatin deficiency (disorder) Has interpretation True Impaired Inferred relationship Some 6
Intellectual disability, epilepsy, extrapyramidal syndrome Has interpretation True Impaired Inferred relationship Some 7
WW domain containing adaptor with coiled-coil-related facial dysmorphism, developmental delay, behavioral abnormalities syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 3
VPS11-related autosomal recessive hypomyelinating leukodystrophy Has interpretation True Impaired Inferred relationship Some 5
Seizures, scoliosis, macrocephaly syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 7
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder) Has interpretation True Impaired Inferred relationship Some 6
Short stature, brachydactyly, obesity, global developmental delay syndrome Has interpretation True Impaired Inferred relationship Some 6
Spastic paraplegia, severe developmental delay, epilepsy syndrome Has interpretation True Impaired Inferred relationship Some 7
Progressive spondyloepimetaphyseal dysplasia, short stature, short fourth metatarsals, intellectual disability syndrome Has interpretation True Impaired Inferred relationship Some 7
Macrocephaly, intellectual disability, neurodevelopmental disorder, small thorax syndrome Has interpretation True Impaired Inferred relationship Some 6
Macrocephaly, intellectual disability, left ventricular non compaction syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 6
Basel Vanagaite Smirin Yosef syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 3
Skeletal dysplasia, T-cell immunodeficiency, developmental delay syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 5
Intellectual disability, seizures, abnormal gait, facial dysmorphism syndrome Has interpretation True Impaired Inferred relationship Some 3
Congenital cerebellar ataxia due to RNA, U12 small nuclear mutation (disorder) Has interpretation True Impaired Inferred relationship Some 3
Severe neurodevelopmental disorder with feeding difficulties, stereotypic hand movement, bilateral cataract Has interpretation True Impaired Inferred relationship Some 8
Metopic ridging, ptosis, facial dysmorphism syndrome Has interpretation True Impaired Inferred relationship Some 4
Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 3
CHD3-related developmental delay, speech delay, intellectual disability, abnormalities of vision, facial dysmorphism syndrome Has interpretation True Impaired Inferred relationship Some 4
Sanjad Sakati syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 6
X-linked microcephaly, growth retardation, prognathism, cryptorchidism syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 6
Severe intellectual disability, hypotonia, strabismus, coarse face, planovalgus syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 5
Intellectual disability, expressive aphasia, facial dysmorphism syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 4
Severe oculo-renal-cerebellar syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 9
Severe oculo-renal-cerebellar syndrome (disorder) Has interpretation False Impaired Inferred relationship Some 10
Fryns Smeets Thiry syndrome Has interpretation True Impaired Inferred relationship Some 2
Fryns Smeets Thiry syndrome Has interpretation True Impaired Inferred relationship Some 3
Progressive cerebello-cerebral atrophy (disorder) Has interpretation True Impaired Inferred relationship Some 6
Progressive cerebello-cerebral atrophy (disorder) Has interpretation True Impaired Inferred relationship Some 7
SATB2-associated syndrome Has interpretation True Impaired Inferred relationship Some 3
SATB2-associated syndrome Has interpretation True Impaired Inferred relationship Some 4
Periprosthetic aortic valve regurgitation Has interpretation True Impaired Inferred relationship Some 2
Sagliker syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 2
Behavioral disturbance due to multi-infarct dementia Has interpretation True Impaired Inferred relationship Some 1
Right ventricular failure due to pulmonary disease Has interpretation True Impaired Inferred relationship Some 3
Right ventricular failure due to pulmonary vascular disease Has interpretation True Impaired Inferred relationship Some 3
Right ventricular failure due to right ventricular infarction (disorder) Has interpretation True Impaired Inferred relationship Some 3
Right ventricular failure due to valvular heart disease Has interpretation True Impaired Inferred relationship Some 3
Renal osteodystrophy due to hyperparathyroidism (disorder) Has interpretation True Impaired Inferred relationship Some 5
Impaired tissue integrity Has interpretation True Impaired Inferred relationship Some 1
Impairment of integrity of oral mucous membrane (finding) Has interpretation True Impaired Inferred relationship Some 1
Autosomal dominant deafness with onychodystrophy syndrome Has interpretation True Impaired Inferred relationship Some 6
Autosomal dominant deafness with onychodystrophy syndrome Has interpretation True Impaired Inferred relationship Some 7
Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 1
Agenesis of corpus callosum, macrocephaly, hypertelorism syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 2
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 6
Severe intellectual disability, agenesis of corpus callosum, facial dysmorphism, cerebellar ataxia syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 7
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Has interpretation True Impaired Inferred relationship Some 5
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Has interpretation True Impaired Inferred relationship Some 6
PHIP-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome Has interpretation True Impaired Inferred relationship Some 3
PHIP-related behavioural problems, intellectual disability, obesity, dysmorphic features syndrome Has interpretation True Impaired Inferred relationship Some 4
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 2
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 6
Incomplete induced termination of pregnancy complicated by renal failure Has interpretation True Impaired Inferred relationship Some 4
Impaired response to stem cell mobilization procedure (finding) Has interpretation True Impaired Inferred relationship Some 1
Renal failure due to and following complete induced termination of pregnancy Has interpretation True Impaired Inferred relationship Some 3
Impaired ability to manage medication regime (finding) Has interpretation True Impaired Inferred relationship Some 1
Faecal incontinence following creation of ileo-anal pouch Has interpretation True Impaired Inferred relationship Some 1
Cardiac tamponade following operative procedure (disorder) Has interpretation True Impaired Inferred relationship Some 2
Profound hearing loss Has interpretation True Impaired Inferred relationship Some 1
Profound sensorineural hearing loss Has interpretation True Impaired Inferred relationship Some 1
Albinism-deafness syndrome of Tietz (disorder) Has interpretation True Impaired Inferred relationship Some 3
Psychogenic urinary incontinence Has interpretation True Impaired Inferred relationship Some 1
Cognitive impairment caused by ethanol (disorder) Has interpretation True Impaired Inferred relationship Some 2
Cross syndrome Has interpretation True Impaired Inferred relationship Some 1
Cross syndrome Has interpretation True Impaired Inferred relationship Some 2
Microcephalus with brachydactyly and kyphoscoliosis syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 9
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome Has interpretation True Impaired Inferred relationship Some 4
X-linked intellectual disability, cerebellar hypoplasia, spondyloepiphyseal dysplasia syndrome Has interpretation True Impaired Inferred relationship Some 5
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 5
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 6
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder) Has interpretation True Impaired Inferred relationship Some 9
NK6 homeobox 2-related autosomal recessive hypomyelinating leukodystrophy (disorder) Has interpretation True Impaired Inferred relationship Some 10
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome Has interpretation True Impaired Inferred relationship Some 6
Neurodevelopmental delay, seizures, ophthalmic anomalies, osteopenia, cerebellar atrophy syndrome Has interpretation True Impaired Inferred relationship Some 7
Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 3
Intellectual disability, autism, speech apraxia, craniofacial dysmorphism syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 4
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 6
Infantile hypotonia, oculomotor anomalies, hyperkinetic movements, developmental delay syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 7
QRICH1-related intellectual disability, chondrodysplasia syndrome Has interpretation True Impaired Inferred relationship Some 4
QRICH1-related intellectual disability, chondrodysplasia syndrome Has interpretation True Impaired Inferred relationship Some 5
Keppen Lubinsky syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 4
Keppen Lubinsky syndrome (disorder) Has interpretation True Impaired Inferred relationship Some 5

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