MeSH Browser

MeSH Supplementary: Erythrocytosis, Familial, 2
Unique ID: C563918
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563918
Entry Term(s): Erythrocytosis, Autosomal Recessive Benign; Polycythemia, Chuvash Type; Polycythemia, VHL-Dependent
Registry Number: 0
Heading Mapped to: Polycythemia / *congenital
Frequency: 6
Note: PROM
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Erythrocytosis, Familial, 2 MeSH Supplementary Concept Data 2024