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"

9 matching diseasesClear search ×

Hairy cell leukemia variant

Prolymphocytic variant of HCL · Prolymphocytic variant of hairy cell leukemia

ORPHA:300878

Acute lymphoblastic leukemia

ALL · Acute lymphoblastic leukemia/lymphoma

ORPHA:513

B-cell chronic lymphocytic leukemia

B-cell chronic lymphoid leukemia · B-CLL

ORPHA:67038

B-cell prolymphocytic leukemia

B-PLL

ORPHA:86852

Classic hairy cell leukemia

HCL-C · Leukemic reticuloendotheliosis

ORPHA:58017

Lymphocytic hypereosinophilic syndrome

HES-L · Lymphocytic variant HES

ORPHA:314970

Precursor B-cell acute lymphoblastic leukemia

B-ALL · Precursor B-cell acute lymphoblastic leukemia/lymphoma

ORPHA:99860

Precursor T-cell acute lymphoblastic leukemia

Precursor T-cell acute lymphoblastic leukemia/lymphoma · Precursor T-cell acute lymphocytic leukemia

ORPHA:99861

T-cell prolymphocytic leukemia

T-PLL · T-cell chronic lymphocytic leukemia

ORPHA:86871