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Metadata
ID DOID:0111487
Name combined oxidative phosphorylation deficiency 7
Definition A combined oxidative phosphorylation deficiency that has_material_basis_in homozygous or compound heterozygous mutation in C12orf65 on chromosome 12q24.31.
https://www.ncbi.nlm.nih.gov/pubmed/20598281
Xrefs

MIM:613559

ORDO:254930

Subsets

DO_rare_slim

Synonyms

COXPD7 [EXACT]

severe C12ORF65-related combined oxidative phosphorylation defect [EXACT]

severe C12ORF65-related COXPD [EXACT]

Parent Relationships

is_a combined oxidative phosphorylation deficiency

is_a autosomal recessive disease

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