OBO ID: DOID:0080290 |
Term Name: | familial erythrocytosis 5 | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0080290 ) |
OTHER familial erythrocytosis 5 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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