(Q9390344)

English

Sheldon-Hall syndrome

human disease

distal arthrogryposis type 2B
Freeman-Sheldon syndrome variant

In more languages

Statements

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class of disease

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distal arthrogryposis

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

health specialty

medical genetics

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genetic association

1 reference

Mutations in TNNT3 cause multiple congenital contractures: a second locus for distal arthrogryposis type 2B

1 reference

Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes

http://purl.obolibrary.org/obo/DOID_0111599

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0111599

1 reference

Identifiers.org

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

Commons category

Sheldon-Hall syndrome

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Identifiers

MeSH descriptor ID

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Disease Ontology ID

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

GARD rare disease ID

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ICD-11 (foundation)

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Medical Dictionary for Regulatory Activities ID

1 reference

https://cdn.who.int/media/docs/default-source/classification/icd/icd-10/icd-10-to-meddra-map---june-2023---codes-mapping.xlsx

based on heuristic

inferred by common ICD-10 mappings on Wikidata and on source

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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(1 entry)

commonswiki Category:Sheldon-Hall syndrome

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