autosomal dominant myoglobinuria
Findings
No curated finding names autosomal dominant myoglobinuria yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Autosomal dominant myoglobinuria is a rare metabolic myopathy characterized by episodic myalgia with myoglobinuria which is induced by fever, viral or bacterial infection, prolonged exercise or alcohol abuse, and could, on occasion, lead to acute renal failure. Between episodes, patients may be asymptomatic or could present elevated creatine kinase levels and mild muscle weakness. There have been no further descriptions in the literature since 1997.
Definition from the Mondo Disease Ontology (MONDO:0008046), read 2026-09-29. CC BY 4.0.
Where it sits
Other names
1 name
Resolves to: autosomal dominant myoglobinuria
- Also called
- myoglobinuria, autosomal dominant