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Browse Orphanet-curated rare diseases with HPO phenotype annotations, synonyms, and linked support programs. Search by name, abbreviation, or synonym.
Try: "IgA nephropathy", "C3G", "Berger's disease", "PKU", "Duchenne"
Primary familial polycythemia
Congenital erythrocytosis due to erythropoietin receptor mutation · Congenital polycythemia due to erythropoietin receptor mutation
Chuvash erythrocytosis
Chuvash polycythemia · Von Hippel-Lindau-dependent polycythemia
Congenital secondary polycythemia
Congenital secondary erythrocytosis
Familial angiolipomatosis
Familial cylindromatosis
Turban tumor syndrome
Familial thrombocytosis
Familial thrombocythemia · Hereditary thrombocythemia
Gaisböck syndrome
Stress erythrocytosis · Stress polycythemia
Polycythemia vera
Acquired primary erythrocytosis · Osler-Vaquez disease