(Q55345896)

English

spinocerebellar ataxia type 41

human disease

SPINOCEREBELLAR ATAXIA 41; SCA41
SPINOCEREBELLAR ATAXIA 41
SCA41
Spinocerebellar Ataxia type 41
cerebellar ataxia type 41

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

autosomal dominant cerebellar ataxia type III

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

spinocerebellar ataxia

1 reference

Disease Ontology

29 November 2021

Disease Ontology ID

genetic association

2 references

UniProt protein ID

13 August 2019

Do mutations in the murine ataxia gene TRPC3 cause cerebellar ataxia in humans?

http://www.orpha.net/ORDO/Orphanet_458798

0 references

http://purl.obolibrary.org/obo/DOID_0111744

1 reference

Disease Ontology

29 November 2021

Disease Ontology ID

http://identifiers.org/doid/DOID:0111744

1 reference

Identifiers.org

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

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

29 November 2021

Disease Ontology ID

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

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

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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