Human Disease Ontology

Last uploaded: March 2, 2018
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:614654

OMIM:614651

OMIM:612016

OMIM:614650

OMIM:614652

OMIM:607426

definition

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

has_exact_synonym

COENZYME Q10 DEFICIENCY, PRIMARY

has_obo_namespace

disease_ontology

id

DOID:0050730

label

coenzyme Q10 deficiency disease

notation

DOID:0050730

prefLabel

coenzyme Q10 deficiency disease

treeView

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

subClassOf

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

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http://purl.obolibrary.org/obo/DOID_0050730 BioAssay Ontology LOOM
http://purl.obolibrary.org/obo/DOID_0050730 BioAssay Ontology SAME_URI
http://purl.obolibrary.org/obo/DOID_0050730 Monarch Disease Ontology SAME_URI
http://purl.obolibrary.org/obo/DOID_0050730 Neuroscience Information Framework (NIF) Standard Ontology LOOM
http://purl.obolibrary.org/obo/DOID_0050730 Neuroscience Information Framework (NIF) Standard Ontology SAME_URI
http://purl.obolibrary.org/obo/DOID_0050730 Monarch Disease Ontology SAME_URI