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"

6 matching diseasesClear search ×

Secondary hypereosinophilic syndrome

HES-R · Reactive hypereosinophilic syndrome

ORPHA:314962

Hypereosinophilic syndrome

HES

ORPHA:168956

Idiopathic hypereosinophilic syndrome

ORPHA:3260

Lymphocytic hypereosinophilic syndrome

HES-L · Lymphocytic variant HES

ORPHA:314970

Primary hypereosinophilic syndrome

Clonal hypereosinophilic syndrome · HES-M

ORPHA:314950

Secondary hemophagocytic lymphohistiocytosis

Acquired hemophagocytic lymphohistiocytosis · Hemophagocytic lymphohistiocytosis

ORPHA:158041