MeSH Browser

MeSH Supplementary: Eosinophilia, Familial
Unique ID: C562722
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562722
Entry Term(s): Familial eosinophilia
Registry Numbers: 0
Heading Mapped to: *Eosinophilia
Frequency: 14
Note: Rare hereditary peripheral eosinophilia characterized by peripheral hypereosinophilia (greater than 500 EOSINOPHILS/micro liter of blood) with or without other organ involvement. Maps to Chromosome 5q. OMIM: 131400
Date of Entry: 2012/11/05
Revision Date: 2016/09/29

Eosinophilia, Familial MeSH Supplementary Concept Data 2025