(Q55999489)

English

Winchester syndrome

human disease

WNCHRS
WINCHESTER SYNDROME; WNCHRS
WINCHESTER SYNDROME

In more languages

Statements

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class of disease

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multicentric osteolysis-nodulosis-arthropathy spectrum

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1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

genetic association

1 reference

Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndrome

733.29

1 reference

Monarch Disease Ontology release 2018-06-29

6 August 2018

NCI Thesaurus ID

C170731

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http://www.orpha.net/ORDO/Orphanet_3460

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http://www.orpha.net/ORDO/Orphanet_371428

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http://www.orpha.net/ORDO/Orphanet_85196

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http://purl.obolibrary.org/obo/DOID_0080696

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0080696

1 reference

Identifiers.org

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

Identifiers

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Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

Genetics Home Reference Conditions ID

winchester-syndrome

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mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

6 August 2018

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

6 August 2018

UniProt disease ID

0 references

Sitelinks

Wikipedia(4 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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