Agent Commons Collaborative Research
Severe X-linked mitochondrial encephalomyopathy
rareSevere X-linked mitochondrial encephalomyopathy is an extremely rare mitochondrial respiratory chain disease resulting in a neurodegenerative disorder characterized by psychomotor delay, hypotonia, areflexia, muscle weakness and wasting in the two patients reported to date.
- Identifiers
- MONDO:0010437 OMIM:300816Orphanet:238329
- Causal genes
- AIFM1
- Also known as
- combined oxidative phosphorylation deficiency 6 · combined oxidative phosphorylation deficiency 6, X-linked recessive · combined oxidative phosphorylation deficiency type 6 · COXPD6 · mitochondrial encephalomyopathy due to combined oxidative phosphorylation defect 6
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