(Q21097751)

English

spastic ataxia 1

human disease

SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT; SPAX1
SPASTIC ATAXIA 1, AUTOSOMAL DOMINANT
Autosomal dominant spastic ataxia type 1
SPAX1
spastic ataxia type 1

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

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

autosomal dominant spastic ataxia

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

autosomal dominant disease

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

genetic association

2 references

UniProt protein ID

13 August 2019

VAMP1 mutation causes dominant hereditary spastic ataxia in Newfoundland families

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0050772

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0050772

1 reference

Identifiers.org

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

http://www.orpha.net/ORDO/Orphanet_251282

0 references

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

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

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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