BioAssay Ontology

Last uploaded: February 21, 2024
Preferred Name

coenzyme Q10 deficiency disease

Synonyms

COENZYME Q10 DEFICIENCY, PRIMARY

Definitions

A mitochondrial metabolism disease that is characterized by a deficiency of CoQ10 resulting from reduced biosynthesis.

ID

http://purl.obolibrary.org/obo/DOID_0050730

created_by

lschriml

creation_date

2012-07-17T12:58:37Z

database_cross_reference

OMIM:PS607426

GARD:10423

has exact synonym

COENZYME Q10 DEFICIENCY, PRIMARY

has_obo_namespace

disease_ontology

id

DOID:0050730

imported from

http://purl.obolibrary.org/obo/doid.owl

label

coenzyme Q10 deficiency disease

notation

DOID:0050730

prefLabel

coenzyme Q10 deficiency disease

textual definition

A mitochondrial metabolism disease that is characterized by a deficiency of CoQ10 resulting from reduced biosynthesis.

subClassOf

http://purl.obolibrary.org/obo/DOID_700

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The BioAssay Ontology integrates with OntoloBridge, allowing community users to suggest additions to the public ontology. Complete the template below to submit a term request directly to the ontology maintainer.

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Example: tissue-based format

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A brief definition, description, or usage of your suggested term. Additional term synonyms may be listed in this section.
Example: Involves the use of a tissue derived from a living organism and is a heterogeneous assay type.

Superclass (required)
The parent term of the suggested term. The parent term should be an existing entry of the current ontology. The superclass can be selected directly from the 'Classes' viewer on Bioportal's left tree navigation.
Example: assay format

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