Cryoglobulinemia, Familial Mixed MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Cryoglobulinemia, Familial Mixed
Unique ID: C565141
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565141
Entry Term(s): Meltzer Syndrome
Registry Number: 0
Heading Mapped to: *Cryoglobulinemia; *Genetic Diseases, Inborn
Frequency: 4
Date of Entry: 2012/11/05

Cryoglobulinemia, Familial Mixed Preferred

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