(Q21097761)

English

spastic ataxia 7

Human disease

Spastic Ataxia With Congenital Miosis
spastic ataxia type 7
SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT
SPASTIC ATAXIA 7, AUTOSOMAL DOMINANT; SPAX7
Autosomal dominant spastic ataxia type 7
Miosis, Congenital, With Spastic Ataxia
SPAX7

In more languages

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

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

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0050945

1 reference

Disease Ontology

30 November 2020

Disease Ontology ID

http://identifiers.org/doid/DOID:0050945

1 reference

Identifiers.org

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

http://www.orpha.net/ORDO/Orphanet_1182

0 references

Identifiers

MeSH descriptor ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

3 July 2018

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

Sitelinks

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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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