(Q16662567)

English

inherited prion disease

instance of prion disease that is caused by an inherited modification of the individual's genome

Familial prion disease
hereditary prion disease

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Statements

instance of

class of disease

0 references

subclass of

transmissible spongiform encephalopathy

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

3 July 2018

Mondo ID

MONDO_0017234

genetic neurodegenerative disease with dementia

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

retrieved

3 July 2018

Mondo ID

MONDO_0017234

nervous system heredodegenerative disease

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

http://www.orpha.net/ORDO/Orphanet_280400

0 references

Identifiers

Google Knowledge Graph ID

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

retrieved

3 July 2018

Mondo ID

MONDO_0017234

ICD-11 ID (Foundation)

542527938

0 references

ICD-11 ID (MMS)

8E02

subject named as

Genetic prion diseases

0 references

0 references

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

1 reference

inferred by common Orphanet mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

16 June 2023

Sitelinks

Wikipedia(1 entry)

frwiki Maladies génétiques à prion

(Q16662567)

inherited prion disease

Statements

Identifiers

Sitelinks

Wikipedia(1 entry)

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