Search Ontology:
Human Disease

combined oxidative phosphorylation deficiency 27

Term ID
DOID:0111489
Synonyms
  • COXPD27
Definition
A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the CARS2 gene on chromosome 13q34. (2)
References
Ontology
Human Disease   ( DOID:0111489 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models