sindromo de Waardenburg
Etoso
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genetic condition involving hearing loss and depigmentation
nomita laŭ
Petrus Johannes Waardenburg
medicina fako
en fokuslisto de Vikimedia projekto
VikiProjekto:Medicino
comorbidity
premature greying of hair[12]
numero en Terminaro de Nacia Kancera Instituto de Usono
C85222[3]
plene kongruas kun
Komuneja kategorio
Waardenburg syndrome
Referenco
- ↑ Freebase Data Dumps, 28 okt. 2013
- ↑ https://github.com/JohnMarkOckerbloom/ftl/blob/master/data/wikimap, 3 apr. 2019
- ↑ 3,0 3,1 3,2 3,3 3,4 3,5 3,6 Disease Ontology, 15 maj. 2019, DOID:9258
- ↑ Quora
- ↑ KBpedia, 9 jul. 2020
- ↑ Orphanet Rare Disease Ontology, https://www.orpha.net/consor/cgi-bin//OC_Exp.php?lng=EN&Expert=3440
- ↑ 7,0 7,1 7,2 7,3 Disease Ontology, 29 nov. 2020, DOID:9258
- ↑ OpenAlex, 26 jan. 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ Nacia Biblioteko de Israelo
- ↑ Phenocarta release 2016-02-04, https://omim.org/entry/277580, http://www.chibi.ubc.ca/Gemma/phenotypes.html?phenotypeUrlId=DOID_9258&geneId=39437, 23 mar. 2016
- ↑ Waardenburg's syndrome patients have mutations in the human homologue of the Pax-3 paired box gene
- ↑ https://omim.org/entry/139100
- ↑ Identifiers.org, https://registry.identifiers.org/registry/doid