Search Ontology:
Human Disease

combined oxidative phosphorylation deficiency 57

Term ID
DOID:0070430
Synonyms
  • COXPD57
Definition
A combined oxidative phosphorylation deficiency that has_material_basis_in compound heterozygous or homozygous mutation in the CRLS1 gene on chromosome 20p12. https://pubmed.ncbi.nlm.nih.gov/35147173/
References
Ontology
Human Disease   ( DOID:0070430 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models