ostéoporose
fragilité excessive du squelette
egzanp nan
classe de maladie
aspect de
santé des femmes
prononciation (fichier son)
langue de l'œuvre, du nom ou du terme: oriya
spécialité médicale
rhumatologie
décrit par
Meyers Konversations-Lexikon, 4e édition (1885–1890)
affirmation détaillée dans: Q112791346, Q123858665
projet Wikimédia s’intéressant à l'élément
Projet:Médecine
identifiant WordLift
identifiant Classification internationale des soins primaires
L95
identifiant NCI Thesaurus
C3298[5]
correspondance exacte
catégorie Commons
Osteoporosis
Referans
- ↑ Monarch Disease Ontology release 2018-06-29, MONDO_0005298, 28 jiyè 2018
- ↑ BBC Things
- ↑ Nuovo soggettario, https://thes.bncf.firenze.sbn.it/termine.php?id=21542, 14 jen 2021
- ↑ 4,0 4,1 4,2 4,3 4,4 4,5 et 4,6 Monarch Disease Ontology release 2018-06-29, 28 jiyè 2018, MONDO_0005298
- ↑ 5,0 5,1 5,2 5,3 5,4 et 5,5 ontologie des maladies, 15 me 2019, DOID:11476
- ↑ National Library pèp Izrayèl
- ↑ sauvegarde de la base de données Freebase, 28 oktòb 2013
- ↑ Gemeinsame Normdatei
- ↑ inferred by common MONDO mappings on source and on Wikidata
- ↑ Quora
- ↑ projet de liens YSO-Wikidata, 8 fevriye 2022
- ↑ http://www.patient.co.uk/patientplus/o.htm
- ↑ 13,0 et 13,1 OpenAlex, 26 janvye 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ 14,0 14,1 et 14,2 ontologie des maladies, 29 novanm 2021, DOID:11476
- ↑ bibliothèque nationale centrale de Florence
- ↑ 16,0 16,1 et 16,2 Human Phenotype Ontology release 2018-03-08, 8 oktòb 2018, HP:0000939
- ↑ https://www.wikidata.org/w/index.php?title=Wikidata:Property_proposal/SNOMED_CT_identifier&oldid=741748825
- ↑ Store norske leksikon, 4 jen 2020
- ↑ BabelNet
- ↑ KBpedia, 9 jiyè 2020
- ↑ Faceted Application of Subject Terminology
- ↑ https://lingualibre.org/wiki/Q636441
- ↑ N0000146043, 13 desanm 2016, NDF-RT, angle
- ↑ Phenocarta, Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11476&ncbiId=2122, http://www.genome.gov/gwastudies/index.cfm?gene=MECOM, 25 me 2020
- ↑ Phenocarta, Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11476&ncbiId=501, http://www.genome.gov/gwastudies/index.cfm?gene=ALDH7A1, 25 me 2020
- ↑ Phenocarta, Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males, https://gemma.msl.ubc.ca/phenotypes.html?phenotypeUrlId=DOID_11476&ncbiId=55553, http://www.genome.gov/gwastudies/index.cfm?gene=SOX6, 25 me 2020
- ↑ P04628, 13 out 2019, UniProt
- ↑ Q9BXB1, 13 out 2019, UniProt
- ↑ O75197, 13 out 2019, UniProt
- ↑ P13797, 13 out 2019, UniProt
- ↑ P02452, 13 out 2019, UniProt
- ↑ https://www.medicalrecords.com/health-a-to-z/osteoporosis-definition/
- ↑ Identifiers.org, https://registry.identifiers.org/registry/doid