Search Ontology:
Human Disease
familial erythrocytosis 5
- Term ID
- DOID:0080290
- Synonyms
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- ECYT5
- Definition
- A primary polycythemia characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the EPO gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/29514032
- References
- Ontology
- Human Disease ( DOID:0080290 )
- is a type of
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