myoglobinuria, acute recurrent, autosomal recessive (Q55998732)
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human disease
- Myoglobinuria, Familial Paroxysmal Paralytic
- Rhabdomyolysis, Acute Recurrent
- MYOGLOBINURIA, ACUTE RECURRENT, AUTOSOMAL RECESSIVE
- genetic recurrent myoglobinuria
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | myoglobinuria, acute recurrent, autosomal recessive |
human disease |
|
Statements
1 reference
3 references
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference