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Myoglobinuria, Acute Recurrent, Autosomal Recessive MeSH Supplementary Concept Data 2024


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 Number
0
Heading Mapped to
*Myoglobinuria
Frequency
8
Date of Entry
2012/11/05
Myoglobinuria, Acute Recurrent, Autosomal Recessive Preferred
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