(Q55345914)

English

cerebellar ataxia type 43

human disease

Spinocerebellar Ataxia type 43
SCA43
Spinocerebellar Ataxia 43

In more languages

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

class of disease

0 references

spinocerebellar ataxia

2 references

Monarch Disease Ontology release 2018-06-29

3 July 2018

Disease Ontology

29 November 2021

Disease Ontology ID

genetic association

2 references

UniProt protein ID

13 August 2019

MME mutation in dominant spinocerebellar ataxia with neuropathy (SCA43).

http://purl.obolibrary.org/obo/DOID_0111745

1 reference

Disease Ontology

29 November 2021

Disease Ontology ID

http://identifiers.org/doid/DOID:0111745

1 reference

Identifiers.org

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

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

29 November 2021

Disease Ontology ID

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

UniProt disease ID

0 references

Sitelinks

Wikipedia(0 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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