Myoglobinuria, Acute Recurrent, Autosomal Recessive (ARARM)

Myoglobinuria, Acute Recurrent, Autosomal Recessive, also known as myoglobinuria, familial paroxysmal paralytic, is related to myoglobinuria and myoglobinuria, recurrent, and has symptoms including muscle weakness and myalgia. An important gene associated with Myoglobinuria, Acute Recurrent, Autosomal Recessive is LPIN1 (Lipin 1). Affiliated tissues include skeletal muscle and kidney, and related phenotypes are muscle weakness and elevated circulating creatine kinase concentration