(Q17120550)

English

peeling skin syndrome

Human disease

Pelvic Organ Prolapse, Susceptibility To, type 2
Pvop2
PELVIC ORGAN PROLAPSE, SUSCEPTIBILITY TO, 2

In more languages

edit

Statements

0 references

0 references

1 reference

29 November 2020

0 references

0 references

1 reference

Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease

on focus list of Wikimedia project

WikiProject Medicine

0 references

exact match

http://purl.obolibrary.org/obo/DOID_0060283

1 reference

29 November 2020

http://identifiers.org/doid/DOID:0060283

1 reference

stated in

Identifiers.org

reference URL

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

http://www.orpha.net/ORDO/Orphanet_263543

0 references

Identifiers

0 references

1 reference

29 November 2020

0 references

1 reference

28 August 2019

Microsoft Academic ID

0 references

0 references

1 reference

28 August 2019

1 reference

28 August 2019

1 reference

28 August 2019

0 references

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

inferred by common Orphanet mappings on source and on Wikidata

16 June 2023

1 reference

inferred by common Orphanet mappings on source and on Wikidata

stated in

UMLS 2023

retrieved

16 June 2023

(Q17120550)

peeling skin syndrome

Statements

Identifiers

Sitelinks

Wikipedia(3 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)