Metadata | |
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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 | |
Subsets |
DO_rare_slim |
Synonyms |
COXPD7 [EXACT] severe C12ORF65-related combined oxidative phosphorylation defect [EXACT] severe C12ORF65-related COXPD [EXACT] |
Parent Relationships |