Rare Disease Library

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"

8 matching diseasesClear search ×

Primary familial polycythemia

Congenital erythrocytosis due to erythropoietin receptor mutation · Congenital polycythemia due to erythropoietin receptor mutation

ORPHA:90042

Chuvash erythrocytosis

Chuvash polycythemia · Von Hippel-Lindau-dependent polycythemia

ORPHA:238557

Congenital secondary polycythemia

Congenital secondary erythrocytosis

ORPHA:238536

Familial angiolipomatosis

ORPHA:199279

Familial cylindromatosis

Turban tumor syndrome

ORPHA:211

Familial thrombocytosis

Familial thrombocythemia · Hereditary thrombocythemia

ORPHA:71493

Gaisböck syndrome

Stress erythrocytosis · Stress polycythemia

ORPHA:90041

Polycythemia vera

Acquired primary erythrocytosis · Osler-Vaquez disease

ORPHA:729