(Q30989223)

English

myoclonic dystonia 26

human disease

DYT26
DYSTONIA 26, MYOCLONIC
myoclonic dystonia type 26
DYSTONIA 26, MYOCLONIC; DYT26

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Statements

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class of disease

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myoclonic dystonia

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

genetic disease

1 reference

Disease Ontology

15 May 2019

Disease Ontology ID

autosomal dominant disease

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

genetic association

2 references

UniProt protein ID

13 August 2019

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0090036

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0090036

1 reference

Identifiers.org

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

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

UniProt disease ID

0 references

Sitelinks

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Wikinews(0 entries)

Wikiquote(0 entries)

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Wikiversity(0 entries)

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Wiktionary(0 entries)

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