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68245003: Spongy degeneration (morphologic abnormality)

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
113357014 Spongy degeneration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
113358016 Spongiform change en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
113359012 Status spongiosus en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
808059016 Spongy degeneration (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
273151000077110 dégénérescence spongieuse 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
Spongy degeneration Is a dégénérescence false Inferred relationship Some
Spongy degeneration Is a Degenerative abnormality true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Variant Creutzfeldt-Jakob disease (disorder) Associated morphology False Spongy degeneration Inferred relationship Some 1
Scrapie Associated morphology False Spongy degeneration Inferred relationship Some 1
Bovine spongiform encephalopathy Associated morphology False Spongy degeneration Inferred relationship Some 1
Creutzfeldt-Jakob disease Associated morphology False Spongy degeneration Inferred relationship Some 1
Spongy degeneration of central nervous system Associated morphology False Spongy degeneration Inferred relationship Some 1
Kuru Associated morphology False Spongy degeneration Inferred relationship Some 1
Spongiform encephalopathy Associated morphology False Spongy degeneration Inferred relationship Some 1
Prion disease Associated morphology False Spongy degeneration Inferred relationship Some 1
Chronic wasting disease of captive mule deer AND/OR elk Associated morphology False Spongy degeneration Inferred relationship Some 1
Gerstmann-Straussler-Scheinker syndrome Associated morphology False Spongy degeneration Inferred relationship Some 1
Transmissible mink encephalopathy Associated morphology False Spongy degeneration Inferred relationship Some 1
Fatal familial insomnia Associated morphology False Spongy degeneration Inferred relationship Some 1
Progressive subcortical gliosis Associated morphology False Spongy degeneration Inferred relationship Some 1
[X]Dementia in Creutzfeldt-Jakob disease Associated morphology False Spongy degeneration Inferred relationship Some 1
maladie à prion associée au SIDA Associated morphology False Spongy degeneration Inferred relationship Some 1
maladie à prion associée au SIDA Associated morphology False Spongy degeneration Inferred relationship Some 1
Creutzfeldt-Jakob disease Associated morphology True Spongy degeneration Inferred relationship Some 1
Fatal familial insomnia Associated morphology True Spongy degeneration Inferred relationship Some 1
Spongy degeneration of central nervous system Associated morphology True Spongy degeneration Inferred relationship Some 1
Spongiform encephalopathy Associated morphology True Spongy degeneration Inferred relationship Some 1
Transmissible mink encephalopathy Associated morphology False Spongy degeneration Inferred relationship Some 1
Prion disease Associated morphology True Spongy degeneration Inferred relationship Some 1
[X]Dementia in Creutzfeldt-Jakob disease Associated morphology False Spongy degeneration Inferred relationship Some 1
Chronic wasting disease of captive mule deer AND/OR elk Associated morphology False Spongy degeneration Inferred relationship Some 1
Progressive subcortical gliosis Associated morphology True Spongy degeneration Inferred relationship Some 1
Variant Creutzfeldt-Jakob disease (disorder) Associated morphology True Spongy degeneration Inferred relationship Some 1
Kuru Associated morphology False Spongy degeneration Inferred relationship Some 1
Scrapie Associated morphology False Spongy degeneration Inferred relationship Some 1
Bovine spongiform encephalopathy Associated morphology False Spongy degeneration Inferred relationship Some 1
Gerstmann-Straussler-Scheinker syndrome Associated morphology True Spongy degeneration Inferred relationship Some 1
Gerstmann-Straussler-Scheinker syndrome Associated morphology False Spongy degeneration Inferred relationship Some 3
Kuru Associated morphology True Spongy degeneration Inferred relationship Some 3
Gerstmann-Straussler-Scheinker syndrome Associated morphology False Spongy degeneration Inferred relationship Some 2
Creutzfeldt-Jakob disease Associated morphology False Spongy degeneration Inferred relationship Some 3
Prion disease Associated morphology False Spongy degeneration Inferred relationship Some 3
Spongiform encephalopathy Associated morphology False Spongy degeneration Inferred relationship Some 2
Kuru Associated morphology False Spongy degeneration Inferred relationship Some 2
Fatal familial insomnia Associated morphology False Spongy degeneration Inferred relationship Some 3
Variant Creutzfeldt-Jakob disease (disorder) Associated morphology False Spongy degeneration Inferred relationship Some 2
Progressive subcortical gliosis Associated morphology False Spongy degeneration Inferred relationship Some 3
Sporadic Creutzfeldt-Jakob disease (disorder) Associated morphology False Spongy degeneration Inferred relationship Some 2
Variant Creutzfeldt-Jakob disease (disorder) Associated morphology False Spongy degeneration Inferred relationship Some 3
Iatrogenic Jakob-Creutzfeldt disease (disorder) Associated morphology True Spongy degeneration Inferred relationship Some 1
Inherited or familial Creutzfeldt-Jakob disease (fCJD) is a very rare form of genetic prion disease characterized by typical CJD features (rapidly progressive dementia, personality/behavioral changes, psychiatric disorders, myoclonus, and ataxia) with a genetic cause and sometimes a family history of dementia. Associated morphology True Spongy degeneration Inferred relationship Some 1
Familial Alzheimer-like prion disease is an exceedingly rare form of prion disease characterized by the neuropathological features of Alzheimer disease including memory impairment and depression, related to abnormal prion protein (PrP) caused by a gene mutation in PRNP. Patients present with a prolonged, atypical course (absence of myoclonus or ataxia) unlike other forms of prion disease with severe neurofibrillary tangle pathology and high levels of cerebral amyloidosis. Associated morphology True Spongy degeneration Inferred relationship Some 1
Variably protease sensitive prionopathy (disorder) Associated morphology True Spongy degeneration Inferred relationship Some 1
Acquired prion disease (disorder) Associated morphology True Spongy degeneration Inferred relationship Some 1
A rare, autosomal dominant neurological disorder due to truncation mutations of the prion protein gene PRNP (20p13) leading to deposition of prion protein amyloid. Onset is usually in the fourth decade of life and reported clinical manifestations include diarrhea, nausea, autonomic failure (areflexia, weakness), neurogenic bladder and urinary infections. Associated morphology True Spongy degeneration Inferred relationship Some 2
Classical sporadic Creutzfeldt-Jakob disease Associated morphology True Spongy degeneration Inferred relationship Some 1
Creutzfeldt-Jakob Disease caused by human growth hormone Associated morphology True Spongy degeneration Inferred relationship Some 1
Creutzfeldt-Jakob Disease caused by human growth hormone Associated morphology True Spongy degeneration Inferred relationship Some 2
Sporadic infantile bilateral striatal necrosis Associated morphology True Spongy degeneration Inferred relationship Some 1
Creutzfeldt Jakob disease following graft of dura (disorder) Associated morphology True Spongy degeneration Inferred relationship Some 1
Sporadic fatal insomnia Associated morphology True Spongy degeneration Inferred relationship Some 1
Sporadic Creutzfeldt-Jakob disease (disorder) Associated morphology True Spongy degeneration Inferred relationship Some 1

This concept is not in any reference sets

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