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Erythrocytosis, Familial, 2 MeSH Supplementary Concept Data 2022


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 Preferred
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