Search Ontology:
Human Disease

familial erythrocytosis 3

Term ID
DOID:0080338
Synonyms
  • ECYT3
Definition
A primary polycythemia that has_material_basis_in heterozygous mutation in the EGLN1 gene on chromosome 1q42. https://www.ncbi.nlm.nih.gov/pubmed/16407130
References
Ontology
Human Disease   ( DOID:0080338 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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