Autosomal dominant myoglobinuria

Orpha code: 99846OMIM code: 160010

Definicja

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.

Disease data
Klasyfikacja

Disease

Kod ORPHA
99846
Kod OMIM
160010
Kod ICD10
R82.1
Kod ICD11
-

No additional description.

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