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DO Term : familial erythrocytosis 2 [DOID:0060474] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A primary polycythemia that has_material_basis_in homozygous or compound heterozygous mutation in the VHL gene (608537) on chromosome 3p25.
  • synonyms:
  • autosomal recessive benign erythrocytosis,
  • Chuvash polycythemia,
  • Chuvash type polycythemia,
  • OMIM:263400,
  • ORDO:238557,
  • ECYT2,
  • ICD10CM:D75.1,
  • Chuvash erythromatosis,
  • 263400
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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