autismespekterforstyrrelse

Siidosisdoallu ii dorjo eará gielaide.

varhaislapsuudessa alkavia kehityshäiriöitä

Eksterne ressurser

ICD-11-MMS
6A02

namain: Autism spectrum disorder

DSM-5-dávdaklassifikašuvnna gilkor
299.00
Experimental Factor Ontology ID
MeSH-ID
D000067877[2][3]

namain: Autism Spectrum Disorder

Quora-fáddágilkor
YSO-gilkor
PatientsLikeMe condition ID
Open Library emne-ID
DeCS-tunniste
OpenAlex-ID
Australian Thesaurus of Education Descriptors -tunniste
10311

namain: autism spectrum disorders

TUBITAK Sosyal Bilimler Ansiklopedisi ID
idRef-gilkor
Disease Ontology-ID
Namuwiki-tunniste
GitHub-aihe
WikiProjectMed ID
Genetics Home Reference Conditions ID
Store medisinske leksikon ID
TED-fáddágilkor
MeSH-kode
Human Phenotype Ontology-ID
Yle-fáddágilkor
18-261473

namain: autismtt, autismspektrumstörning

ScienceDirect emne-ID
GARD ID
ABC News -aihetunniste
LCAuth-gilkor
Freebase-gilkor
UMLS CUI
ICD-11 (foundation)
BabelNet-id
BNCF
56907

namain: Disturbi dello spettro autistico

også kjent som: Disturbi generalizzati dello sviluppo, Disturbi generalizzati di sviluppo infantile, Disturbi pervasivi dello sviluppo, Disturbi pervasivi dello sviluppo del bambino, DSP

Analysis & Policy Observatory term ID
Encyclopedia of China (Third Edition) ID
55908

namain: 孤独症谱系障碍

25653

namain: 自闭症谱系障碍

BnF-gilkor
16627519x[11]

namain: Troubles envahissants du développement

National Library of Israel J9U ID

lea

nevroutviklingsforstyrrelse
funksjonsnedsettelse
sykdomsklasse

gullá čuovvovaš kategoriijai

pervasive developmental disorder[6]

dieđasuorgi

sociological and cultural aspects of autism
psykiatriija

dálkkasdieđalaš fágasuorgi

psykologiija

dikšumis geavahuvvon dálkkas

TEACCH approach

genetisk assosiasjon

Kaliriini[13][14][15]

bestemmelsesmetode: IMP

čuovvumušat: disease susceptibility

Wikiprošeavtta fáddálisttus

Wikiprojekti:Lääketiede

handled, mitigated, or managed by

autismeterapi[16]

ICPC-2

P99

NCI Thesaurus-id

C88412

eará ášši go

autisma

fáttá váldomálle

Malline:Autismin kirjo

Gáldu

  1. inferred by common DOID mappings on source and on Wikidata
  2. a á b c č Human Phenotype Ontology release 2018-03-08, 8 golggotmánnu 2018, HP:0000729
  3. Disease Ontology, 15 miessemánnu 2019, DOID:0060041
  4. YSOn ja Wikidatan linkitys
  5. a á b OpenAlex, 26 ođđajagimánnu 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  6. a á b Disease Ontology, 30 skábmamánnu 2020, DOID:0060041
  7. https://github.com/topics/autism-spectrum-disorder, autism-spectrum-disorder · GitHub Topics · GitHub, 25 suoidnemánnu 2021
  8. Disease Ontology, 28 borgemánnu 2019, DOID:0060041
  9. Freebase-data fra Google, 28 golggotmánnu 2013
  10. BabelNet
  11. Nuovo soggettario, https://thes.bncf.firenze.sbn.it/termine.php?id=56907, 17 geassemánnu 2021
  12. Israels nasjonalbibliotek
  13. KALRN: a central regulator of synaptic function and synaptopathies, oversiktsartikkel
  14. Both rare and common genetic variants contribute to autism in the Faroe Islands
  15. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
  16. https://www.cdc.gov/ncbddd/autism/treatment.html
  17. Identifiers.org, https://registry.identifiers.org/registry/doid