Myoglobinuria, Autosomal Dominant MeSH Supplementary Concept Data 2022

Details
Concepts

MeSH Supplementary: Myoglobinuria, Autosomal Dominant
Unique ID: C563546
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563546
Registry Number: 0
Heading Mapped to: Myoglobinuria / *congenital
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Myoglobinuria, Autosomal Dominant Preferred

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