(Q3961699)

English

De Barsy syndrome

human disease

cutis laxa-corneal clouding-intellectual disability syndrome
autosomal recessive cutis laxa type III

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Statements

instance of

class of disease

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subclass of

inborn disorder of ornithine or proline metabolism

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1 reference

30 November 2020

autosomal recessive disease

1 reference

30 November 2020

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on focus list of Wikimedia project

WikiProject Medicine

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exact match

http://purl.obolibrary.org/obo/DOID_0070143

1 reference

30 November 2020

http://identifiers.org/doid/DOID:0070143

1 reference

stated in

Identifiers.org

reference URL

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

http://www.orpha.net/ORDO/Orphanet_2962

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Identifiers

MeSH descriptor ID

C535990

2 references

imported from Wikimedia project

28 August 2019

1 reference

30 November 2020

1 reference

imported from Wikimedia project

1 reference

28 August 2019

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ICD-11 ID (Foundation)

1718974486

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Microsoft Academic ID

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1 reference

28 August 2019

1 reference

28 August 2019

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Sitelinks

Wikipedia(5 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)

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