Home
Random
Nearby
Log in
Settings
Donate
About Wikidata
Disclaimers
Search
(Q16662567)
Watch
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
In more languages
edit
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
retrieved
3 July 2018
Mondo ID
MONDO_0017234
exact match
http://www.orpha.net/ORDO/Orphanet_280400
0 references
Identifiers
Google Knowledge Graph ID
/g/1216fdkd
0 references
ICD-10-CM
A81.8
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 July 2018
Mondo ID
MONDO_0017234
ICD-11 (foundation)
542527938
0 references
ICD-11 ID (MMS)
8E02
subject named as
Genetic prion diseases
0 references
Mondo ID
MONDO_0017234
0 references
Orphanet ID
280400
mapping relation type
exact match
1 reference
stated in
Monarch Disease Ontology release 2018-06-29
retrieved
3 July 2018
Mondo ID
MONDO_0017234
UMLS CUI
C5679775
1 reference
based on heuristic
inferred by common Orphanet mappings on source and on Wikidata
stated in
UMLS 2023
retrieved
16 June 2023
Sitelinks
Wikipedia
(1 entry)
edit
frwiki
Maladies génétiques à prion
Wikibooks
(0 entries)
edit
Wikinews
(0 entries)
edit
Wikiquote
(0 entries)
edit
Wikisource
(0 entries)
edit
Wikiversity
(0 entries)
edit
Wikivoyage
(0 entries)
edit
Wiktionary
(0 entries)
edit
Multilingual sites
(0 entries)
edit