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107669003: Degenerative abnormality (morphologic abnormality)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
172105010 Degenerative abnormality en Synonym Active Entire term case insensitive SNOMED CT core module
593391011 Degenerative abnormality (morphologic abnormality) en Fully specified name Active Entire term case insensitive SNOMED CT core module


289 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Degenerative abnormality Is a Morphologically abnormal structure true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Spastic paraplegia with Paget disease of bone syndrome Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 18 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 25 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 10 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 6 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spastic paraplegia with precocious puberty syndrome Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal dominant spastic paraplegia type 29 Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia dysmorphism syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 3
Spinocerebellar ataxia dysmorphism syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 4
Encephalopathy, intracerebral calcification, retinal degeneration syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spastic paraplegia, nephritis, deafness syndrome Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 5
Van den Bosch syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebelloparenchymal disorder type 3 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 3
Autosomal recessive cerebelloparenchymal disorder type 3 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 4
Richards-Rundle syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Richards-Rundle syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 3
Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 3
Autosomal recessive spastic paraplegia type 11 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spastic paraparesis co-occurrent with deafness Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Cochleosaccular degeneration and cataract syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 7 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 7 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 1 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 1 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 2 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 2 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 6 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 6 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 8 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 8 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 10 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 10 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 4 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 4 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spastic paraplegia type 7 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 28 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 28 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 29 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 29 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 31 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 31 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Macrocephaly with spastic paraplegia and dysmorphism syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Primary progressive non fluent aphasia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Primary progressive non fluent aphasia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Logopenic progressive aphasia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Logopenic progressive aphasia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Right temporal atrophy variant frontotemporal dementia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 15/16 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 15/16 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Behavioral variant of frontotemporal dementia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Behavioral variant of frontotemporal dementia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Maternally inherited Leigh syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Infantile striatonigral degeneration Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Congenital lactic acidosis Saguenay-Lac-Saint-Jean type Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Oligoosteoarthritis Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Prolapse of cervical intervertebral disc co-occurrent and due to degeneration Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Degeneration of cervical intervertebral disc co-occurrent with osteophyte of cervical vertebra Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Degeneration of thoracic intervertebral disc without prolapse Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Prolapse of thoracic intervertebral disc co-occurrent and due to degeneration Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Degeneration of thoracic intervertebral disc co-occurrent with osteophyte Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Degeneration of lumbar intervertebral disc without prolapse Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Prolapse of lumbar intervertebral disc co-occurrent and due to degeneration Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Degeneration of lumbar intervertebral disc co-occurrent with osteophyte of lumbar vertebra Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Osteoarthritis of joint of left ankle and/or foot Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Acquired hypoganglionosis of large intestine Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Acquired hypoganglionosis of large intestine Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Autosomal dominant hereditary spastic paraplegia Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 2
Subconjunctival degeneration Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Degeneration of posterior pole of eye Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Degeneration of iris Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spastic paraplegia, glaucoma, intellectual disability syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 4
Spinocerebellar ataxia type 40 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 40 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Spinocerebellar ataxia type 38 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Spinocerebellar ataxia type 38 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Degeneration of spine Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Osteoarthritis of facet joint of thoracic spine Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Osteoarthritis of lumbar spinal facet joint Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Lumbosacral spondylosis co-occurrent with root compression Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 1
Severe intellectual disability and progressive spastic paraplegia Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 27 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Primary non-essential cutis verticis gyrata Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia Associated morphology False Degenerative abnormality Inferred relationship Existential restriction modifier 2
Autosomal dominant spastic paraplegia type 3 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Gemignani syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Circumferential viscodilation and tensioning of sinus venosus of sclera by external approach Procedure morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 69 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 71 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal spastic paraplegia type 72 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 60 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Autosomal recessive spastic paraplegia type 66 Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Infantile cerebellar and retinal degeneration Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 1
Infantile cerebellar and retinal degeneration Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2
Brachydactyly, short stature, retinitis pigmentosa syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 3
Autosomal recessive cerebellar ataxia, psychomotor delay syndrome Associated morphology True Degenerative abnormality Inferred relationship Existential restriction modifier 2

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