MeSH Browser

MeSH Supplementary: Myoglobinuria, Acute Recurrent, Autosomal Recessive
Unique ID: C564832
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564832
Entry Term(s): Myoglobinuria, Familial Paroxysmal Paralytic; Rhabdomyolysis, Acute Recurrent
Registry Numbers: 0
Heading Mapped to: *Myoglobinuria
Frequency: 8
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Myoglobinuria, Acute Recurrent, Autosomal Recessive MeSH Supplementary Concept Data 2025