OBO ID: DOID:0080290
Term Name: familial erythrocytosis 5 Search Ontology:
Synonyms:
  • 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)
OTHER familial erythrocytosis 5 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
EPO Erythrocytosis, familial, 5 617907
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None