Erythrocytosis, Familial, 3 MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Erythrocytosis, Familial, 3
Unique ID: C565221
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565221
Registry Numbers: 0
Heading Mapped to: Polycythemia / congenital
Frequency: 0
Note: mutation in EGLN1
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Erythrocytosis, Familial, 3 Preferred

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