(Q26492776)

English

ataxia with oculomotor apraxia type 3

human disease

ataxia-oculomotor apraxia 3
AOA3
Ataxia-Oculomotor Apraxia type 3
ATAXIA-OCULOMOTOR APRAXIA 3; AOA3

In more languages

Statements

class of disease

0 references

autosomal recessive cerebellar ataxia

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

oculomotor apraxia

0 references

spinocerebellar ataxia with axonal neuropathy type 2

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

genetic association

1 reference

UniProt protein ID

13 August 2019

on focus list of Wikimedia project

WikiProject Medicine

0 references

NCI Thesaurus ID

C173403

0 references

http://purl.obolibrary.org/obo/DOID_0060557

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0060557

1 reference

Identifiers.org

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

http://www.orpha.net/ORDO/Orphanet_64753

0 references

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

GARD rare disease ID

0 references

0 references

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

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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