myoglobinuria, acute recurrent, autosomal recessive

Rare Disease

MONDO:0009992

Also known as:

myoglobinuria, acute recurrent, autosomal recessivemyoglobinuria, familial paroxysmal paralyticrhabdomyolysis, acute recurrent

Genes

Clinical Trials

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Newborn Screening

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Patient Groups

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Companies Active in myoglobinuria, acute recurrent, autosomal recessive

0 approved

Organizations with approved therapies for this disease

No approved therapies yet

Research is ongoing — 1 company has orphan drug designations for this disease

Rhone-Poulenc Rorer Pharmaceuticals, Inc.

Other

Designated

View all companies active in myoglobinuria, acute recurrent, autosomal recessive

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