Neidio i'r cynnwys

syndrom Gilles de la Tourette

Ni chefnogir cynnwys y dudalen mewn ieithoedd eraill.

neurodevelopmental condition

testun y ddelwedd: Жорж Жиль де ла Туретт (1859–1904), Georges Gilles de la Tourette, [[Жорж Жыль дэ ля Турэт]] (1857–1904), у гонар якога названы сындром

Adnoddau allanol

ICD-11 ID (MMS)
8A05.00

enwyd fel: Tourette syndrome

dynodwr Encyclopædia Britannica Online
science/Tourette-syndrome

enwyd fel: Tourette syndrome

dynodwr YSA
PatientsLikeMe condition ID
UniProt disease ID
DeCS ID
Ávvir topic ID
DiseasesDB
dynodwr BBC Things
dynodwr BnF
12289322r[2]

enwyd fel: Gilles de la Tourette, Maladie de

subreddit
Tourettes

iaith y gwaith neu'r enw: Saesneg

OmegaWiki Defined Meaning
Mondo ID
dynodwr JSTOR (pwnc)
WikiKids ID
dynodwr NE.se
tourettes-syndrom

enwyd fel: Tourettes syndrom

gilles-de-la-tourettes-syndrom

enwyd fel: Gilles de la Tourettes syndrom

GARD rare disease ID
ICD-10-CM
ICD-9 ID
Encyclopedia of China (Third Edition) ID
Australian Educational Vocabulary ID
National Library of Israel J9U ID
dynodwr Freebase
Experimental Factor Ontology ID
dynodwr Quora
dynodwr YSO
dynodwr KEGG
Baidu Tieba name
抽动症

nifer o weithiau: 332,978

pwynt mewn amser: 3 Ebrill 2023

OpenAlex ID
dynodwr Cultureel Woordenboek
dynodwr KBpedia
Orphanet ID
856[3]

mapping relation type: close match

dynodwr OMIM
Disease Ontology ID
NHS Health A to Z ID
WikiProjectMed ID
Online PWN Encyclopedia ID
Genetics Home Reference Conditions ID
MedlinePlus ID
ICD-11 (foundation)
eMedicine ID
289457

enwyd fel: Pediatric Tourette Syndrome

1182258

enwyd fel: Tourette Syndrome and Other Tic Disorders

dynodwr BBC News (pwnc)
Yle topic ID
dynodwr MeSH
D005879[13]

enwyd fel: Tourette Syndrome

mapping relation type: exact match

ICD-10
dynodwr LCAuth
sh85054937[14]

enwyd fel: Tourette syndrome

dynodwr Wolfram Language (endid)
WikiSkripta article ID
Lille norske leksikon ID
dynodwr thesawrws Senedd y DU
297591

enwyd fel: Tourette's syndrome

dynodwr BabelNet
Store medisinske leksikon ID
dynodwr yn thesawrws y BNCF
UMLS CUI
C1392622[3]

mapping relation type: close match

dynodwr NKC
ph661389

enwyd fel: Tourettův syndrom

GND
Den Store Danske ID
Cod MeSH
ScienceDirect topic ID

enghraifft o'r canlynol

clefyd prin
dosbarth o glefyd

isddosbarth o'r canlynol

tic disorder[12]
genetic movement disorder[3]

enwyd ar ôl

Georges Gilles de la Tourette

arbenigedd meddygol

niwroleg

symtomau

tic

genetic association

PHEX[26]

dull penderfynu: genome-wide association study, TAS

IMMP2L[27]
SLITRK1[28]

ar restr sylw'r prosiect Wikimedia

risk factor

ysmygu[29]

effaith: incidence

has phenotype

tic[4]

ICD-9-CM

307.23[4][3]

dynodwr ICPC 2

P10

Thesawrws NCI

C35078[4]

categori Comin

Tourette syndrome

prif gategori

Category:Tourette syndrome

Cyfeiriadau

  1. BBC Things
  2. Nuovo soggettario, https://thes.bncf.firenze.sbn.it/termine.php?id=33557, 15 Mehefin 2021
  3. 3.0 3.1 3.2 3.3 3.4 3.5 3.6 Monarch Disease Ontology release 2018-06-29, 28 Gorffennaf 2018, MONDO_0007661
  4. 4.0 4.1 4.2 4.3 4.4 4.5 Disease Ontology, 15 Mai 2019, DOID:11119
  5. Llyfrgell Genedlaethol Israel
  6. Freebase Data Dumps, 28 Hydref 2013
  7. inferred by common MONDO mappings on source and on Wikidata
  8. Quora
  9. YSO-Wikidata mapping project
  10. OpenAlex, 26 Ionawr 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  11. KBpedia, 9 Gorffennaf 2020
  12. 12.0 12.1 12.2 Disease Ontology, 30 Tachwedd 2020, DOID:11119
  13. Monarch Disease Ontology release 2018-06-29, MONDO_0007661, 28 Gorffennaf 2018
  14. Gemeinsame Normdatei
  15. BabelNet
  16. National Central Library of Florence
  17. N0000148690, 13 Rhagfyr 2016, NDF-RT, Saesneg
  18. N0000147896, 13 Rhagfyr 2016, NDF-RT, Saesneg
  19. N0000146461, 13 Rhagfyr 2016, NDF-RT, Saesneg
  20. N0000148350, 13 Rhagfyr 2016, NDF-RT, Saesneg
  21. 21.0 21.1 21.2 Drug Indications Extracted from FAERS, 2 Hydref 2018
  22. N0000147968, 13 Rhagfyr 2016, NDF-RT, Saesneg
  23. N0000146801, 13 Rhagfyr 2016, NDF-RT, Saesneg
  24. N0000146207, 13 Rhagfyr 2016, NDF-RT, Saesneg
  25. N0000146289, 13 Rhagfyr 2016, NDF-RT, Saesneg
  26. Phenocarta, Genome-wide association study of Tourette's syndrome, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11119&ncbiId=5251, http://www.genome.gov/gwastudies/index.cfm?gene=PHEX, 25 Mai 2020
  27. Q96T52, 13 Awst 2019, UniProt
  28. Sequence variants in SLITRK1 are associated with Tourette's syndrome
  29. 27566119
  30. Identifiers.org, https://registry.identifiers.org/registry/doid