Combined Oxidative Phosphorylation Deficiency 3 [Supplementary Concept]
mutation in TSFM
Date introduced: November 5, 2012
MeSH Unique ID: C566467
Heading Mapped to:
Entry Terms:
- COXPD3
- Concentric Cardiomyopathy, Hypotonia, And Lactic Acidosis
- Encephalomyopathy, Respiratory Failure, And Lactic Acidosis