107669003: anomalie dégénérative (anomalie morphologique)

SNOMED CT Concept\structure corporelle\structure modifiée sur le plan morphologique\structure anormale sur le plan morphologique\Degenerative abnormality

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
Degenerative abnormality	est un(e) (attribut)	structure anormale sur le plan morphologique	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Juvenile Parkinson's disease	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Orthostatic hypotension co-occurrent and due to Parkinson's disease (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Sporadic Parkinson disease (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Atypical juvenile parkinsonism (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
maladie de Parkinson à début précoce	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Early onset parkinsonism and intellectual disability syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Autosomal dominant late onset Parkinson disease (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Juvenile osteochondrosis of thoracolumbar spine (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
Congenital retinoschisis	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Parkinsonian syndrome with idiopathic orthostatic hypotension (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	5
Rheumatoid arthritis with erosion of joint (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Progressive cerebellar ataxia with hypogonadism	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Cervical spondylosis (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Post-traumatic coxarthrosis, bilateral	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	4
Post-traumatic coxarthrosis, bilateral	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Westphal-Strumpell syndrome	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Westphal-Strumpell syndrome	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Westphal-Strumpell syndrome	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
X-linked complex hereditary spastic paraplegia	morphologie associée (attribut)	False	Degenerative abnormality	Inferred relationship	Some	2
X-linked pure hereditary spastic paraplegia	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive familial Parkinson disease	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Juvenile osteochondrosis of tarsus (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal dominant Alzheimer disease due to mutation of presenilin 2 (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal dominant Alzheimer disease due to mutation of presenilin 1 (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Atypical progressive supranuclear palsy syndrome	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Progressive supranuclear palsy parkinsonism syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Progressive supranuclear palsy progressive non fluent aphasia	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Progressive supranuclear palsy corticobasal syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Felty syndrome with seronegative erosive rheumatoid arthritis (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Degenerating leiomyoma	est un(e) (attribut)	False	Degenerative abnormality	Inferred relationship	Some
Anti-citrullinated protein antibody positive erosive rheumatoid arthritis (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Rheumatoid factor and anti-citrullinated protein antibody positive erosive rheumatoid arthritis	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Seronegative erosive rheumatoid arthritis	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Oligoarticular osteoarthritis (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Psychosis co-occurrent and due to Parkinson's disease (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
Degenerative sequelae of disorders	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Childhood-onset basal ganglia degeneration syndrome	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Kyphoscoliosis, lateral tongue atrophy, hereditary spastic paraplegia syndrome	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive spastic paraplegia type 76 (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Menkes kinky-hair syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Allan-Herndon-Dudley syndrome	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Severe X-linked mitochondrial encephalomyopathy (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
X-linked intellectual disability with hypogammaglobulinemia and progressive neurological deterioration syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Acyl-coenzyme A oxidase deficiency (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Postnatal microcephaly, infantile hypotonia, spastic diplegia, dysarthria, intellectual disability syndrome	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	4
Autosomal recessive spastic paraplegia type 78 (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Degeneration of uterine fibroid	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Deep sclerectomy without spacer (procedure)	morphologie du site d'intervention (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Deep sclerectomy with spacer (procedure)	morphologie du site d'intervention (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Deep sclerectomy (procedure)	morphologie du site d'intervention (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
Deep sclerectomy with collagen implant (procedure)	morphologie du site d'intervention (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder)	morphologie associée (attribut)	False	Degenerative abnormality	Inferred relationship	Some	2
Spinocerebellar ataxia due to vitamin E deficiency (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Spinocerebellar ataxia due to vitamin E deficiency (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Psychomotor regression, oculomotor apraxia, movement disorder, nephropathy syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive spastic paraplegia type 74	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
Spastic paraplegia, severe developmental delay, epilepsy syndrome	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	4
Autosomal dominant hereditary spastic paraplegia	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
X-linked hereditary spastic paraplegia (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive hereditary spastic paraplegia	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Pure hereditary spastic paraplegia	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
Complicated hereditary spastic paraplegia	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
paraplégie spastique autosomique type 30	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive spastic paraplegia type 35	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive spastic paraplegia type 62	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
paraplégie spastique héréditaire (trouble)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Autosomal dominant spastic paraplegia type 36 (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
Spastic paraplegia with Paget disease of bone syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	4
Spastic paraplegia with precocious puberty syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	4
Autosomal dominant spastic paraplegia type 29 (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
Spastic paraplegia, nephritis, deafness syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive complex spastic paraplegia due to Kennedy pathway dysfunction (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	3
X-linked complex hereditary spastic paraplegia	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 12 (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 19	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive spastic paraplegia type 28	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Spastic paraplegia, facial cutaneous lesion syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
paraplégie spastique autosomique dominante type 31	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 42	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 37 (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Intellectual disability, spasticity, ectrodactyly syndrome	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 9A	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 9B	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive spastic paraplegia type 9B	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal dominant spastic paraplegia type 73	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive spastic paraplegia type 75 (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive spastic paraplegia type 77	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Pituitary degeneration	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Leigh syndrome due to cytochrome C oxidase deficiency (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Acute infantile liver failure, cerebellar ataxia, peripheral sensory motor neuropathy syndrome (disorder)	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
atrophie musculaire, ataxie, rétinite pigmentaire et diabète sucré	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	2
Autosomal dominant amyotrophic lateral sclerosis type 1	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Autosomal recessive amyotrophic lateral sclerosis type 1	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1
Amyotrophic lateral sclerosis type 1	morphologie associée (attribut)	True	Degenerative abnormality	Inferred relationship	Some	1

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Id	Description	Lang	Type	Status	Case?	Module
172105010	Degenerative abnormality	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
593391011	Degenerative abnormality (morphologic abnormality)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
65101000077112	anomalie dégénérative	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
687151000077111	anomalie dégénérative (anomalie morphologique)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)