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 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models
Citations