(Q22443995)

English

spinocerebellar ataxia type 31

Human disease

SPINOCEREBELLAR ATAXIA 31; SCA31
Spinocerebellar Ataxia, 16Q22-Linked
SPINOCEREBELLAR ATAXIA 31
Spinocerebellar Ataxia type 31
SCA31

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Statements

instance of

developmental defect during embryogenesis

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

0 references

spinocerebellar ataxia

1 reference

29 November 2020

autosomal dominant cerebellar ataxia type III

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

2 references

13 August 2019

Spinocerebellar ataxia type 31 is associated with "inserted" penta-nucleotide repeats containing (TGGAA)n

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C176901

0 references

exact match

http://purl.obolibrary.org/obo/DOID_0050980

1 reference

29 November 2020

http://identifiers.org/doid/DOID:0050980

1 reference

stated in

Identifiers.org

reference URL

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

http://www.orpha.net/ORDO/Orphanet_217012

0 references

Identifiers

MeSH descriptor ID

C566146

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

1 reference

29 November 2020

0 references

Google Knowledge Graph ID

0 references

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

0 references

1 reference

28 August 2019

mapping relation type

exact match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

mapping relation type

close match

1 reference

stated in

Monarch Disease Ontology release 2018-06-29

3 July 2018

0 references

Sitelinks

Wikipedia(1 entry)

jawiki 脊髄小脳変性症31型

(Q22443995)

spinocerebellar ataxia type 31

Statements

Identifiers

Sitelinks

Wikipedia(1 entry)

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