Familial hyperchylomicronemia syndrome MeSH Supplementary Concept Data 2025

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MeSH Supplementary: Familial hyperchylomicronemia syndrome
Unique ID: C538489
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538489
Entry Term(s): Hyperlipoproteinemia, type 1
Registry Numbers: 0
Heading Mapped to: *Hyperlipoproteinemia Type I
Frequency: 67
Date of Entry: 2010/08/25
Revision Date: 1955/01/01

Familial hyperchylomicronemia syndrome Preferred

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