(Q18592)

genetic neurodegenerative disease with dementia

3 July 2018

Mondo ID

MONDO_0017276

1 reference

3 July 2018

1 reference

30 November 2020

1 reference

30 November 2020

0 references

Pick's disease.png
1,200 × 552; 223 KB

0 references

spoken text audio

Nl-frontotemporale dementie-article.ogg
5 min 17 s; 3.52 MB

language of work or name

Dutch

1 reference

https://nl.wikipedia.org/w/index.php?title=Frontotemporale_dementie&oldid=53373116

Dutch Wikipedia

Wikimedia import URL

has cause

unknown

0 references

health specialty

Neurology, psychiatry, and neuropsychiatry

0 references

symptoms and signs

dementia

1 reference

1 reference

behavioral disorder

3 references

Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP

type of reference

review article

GABRB2, a key player in neuropsychiatric disorders and beyond

anomic aphasia

1 reference

primary progressive aphasia

0 references

language disorder

2 references

Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP

GABRB2, a key player in neuropsychiatric disorders and beyond

type of reference

review article

memory disorder

2 references

Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP

GABRB2, a key player in neuropsychiatric disorders and beyond

type of reference

review article

motor disorder

2 references

Integrative system biology analyses of CRISPR-edited iPSC-derived neurons and human brains reveal deficiencies of presynaptic signaling in FTLD and PSP

GABRB2, a key player in neuropsychiatric disorders and beyond

1 reference

neurological diagnostic techniques

1 reference

magnetic resonance imaging

1 reference

autopsy

1 reference

selective serotonin reuptake inhibitor

possible treatment

1 reference

antipsychotics

1 reference

genetic association

CHMP2B

1 reference

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

on focus list of Wikimedia project

WikiProject Medicine

0 references

prevalence

0.00022

1 reference

The epidemiology of frontotemporal dementia

NCI Thesaurus ID

C84719

exact match

1 reference

http://purl.obolibrary.org/obo/DOID_9255

3 July 2018

1 reference

30 November 2020

http://identifiers.org/doid/DOID:9255

1 reference

https://registry.identifiers.org/registry/doid

Identifiers.org

reference URL

http://purl.obolibrary.org/obo/HP_0002145

1 reference

Human Phenotype Ontology release 2018-03-08

Human Phenotype Ontology ID

8 October 2018

HP:0002145

http://www.orpha.net/ORDO/Orphanet_282

0 references

topic's main category

Category:Frontotemporal dementia

0 references

Identifiers

MeSH descriptor ID

D057180

exact match

subject named as

Frontotemporal Dementia

1 reference

PatientsLikeMe condition ID

3 July 2018

C10.228.140.380.266.299

0 references

C10.574.950.300.299

0 references

C18.452.845.800.300.299

0 references

F03.615.400.380.299

0 references

frontal-lobe-dementia

0 references

BBC Things ID

edb7ef7d-9ae6-4a0a-9e15-4e8e3edab4ed

1 reference

0 references

1 reference

30 November 2020

1 reference

Encyclopedia of China (Third Edition) ID

0 references

1 reference

28 October 2013

1 reference

15 May 2019

1 reference

NBK1371

1 reference

Human Phenotype Ontology ID

HP:0002145

1 reference

Human Phenotype Ontology release 2018-03-08

Human Phenotype Ontology ID

8 October 2018

HP:0002145

ICD-10 ID

G31.0

1 reference

1 reference

3 July 2018

Mondo ID

MONDO_0017276

ICD-11 ID (Foundation)

0 references

0 references

8A23

Frontotemporal lobar degeneration

0 references

ICD-9 ID

331.19

1 reference

JSTOR topic ID (archived)

frontotemporal-dementia

0 references

Medical Dictionary for Regulatory Activities ID

10009204

1 reference

reference URL

https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

0 references

1 reference

15 May 2019

1 reference

15 May 2019

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

26 January 2022

https://docs.openalex.org/download-snapshot/snapshot-data-format

1 reference

15 May 2019

frontotemporal-dementia

1 reference

reference URL

http://www.patient.co.uk/patientplus/f.htm

Store medisinske leksikon ID

frontallappdemens

related match

subject named as

frontallappdemens

1 reference

Great Norwegian Encyclopedia

29 May 2020

UMLS CUI

C4229268

exact match

1 reference