(Q55784979)

English

coenzyme Q10 deficiency, primary, 8; COQ10D8

human disease

COQ10D8
Coenzyme Q10 Deficiency, Primary, type 8
Coenzyme Q10 Deficiency, Primary, 8
primary coenzyme Q10 deficiency 8
coenzyme Q10 deficiency, primary, 8

In more languages

Statements

developmental defect during embryogenesis

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

0 references

1 reference

Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid.

class of disease

0 references

coenzyme Q10 deficiency disease

1 reference

Disease Ontology

29 November 2021

Disease Ontology ID

genetic disease

1 reference

Disease Ontology

29 November 2020

Disease Ontology ID

genetic association

2 references

UniProt protein ID

13 August 2019

Rescue of primary ubiquinone deficiency due to a novel COQ7 defect using 2,4-dihydroxybensoic acid.

on focus list of Wikimedia project

WikiProject Medicine

0 references

http://purl.obolibrary.org/obo/DOID_0070245

1 reference

Disease Ontology

29 November 2021

Disease Ontology ID

http://identifiers.org/doid/DOID:0070245

1 reference

Identifiers.org

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

Identifiers

Disease Ontology ID

1 reference

Disease Ontology

29 November 2021

Disease Ontology ID

0 references

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 July 2018

1 reference

Disease Ontology

28 August 2019

Disease Ontology ID

mapping relation type

1 reference

Monarch Disease Ontology release 2018-06-29

28 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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