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 ×

Juvenile myelomonocytic leukemia

Juvenile chronic myelomonocytic leukemia · JMML

ORPHA:86834

Acute myelomonocytic leukemia

AMMoL · AML M4

ORPHA:517

Atypical chronic myeloid leukemia

Subacute myeloid leukemia

ORPHA:98824

B-cell chronic lymphocytic leukemia

B-cell chronic lymphoid leukemia · B-CLL

ORPHA:67038

Chronic mast cell leukemia

Chronic MCL

ORPHA:566396

Chronic myeloid leukemia

CML · Chronic granulocytic leukemia

ORPHA:521

Chronic myelomonocytic leukemia

CMML

ORPHA:98823

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia

CBL syndrome · Noonan syndrome-like disorder with JMML

ORPHA:363972

T-cell prolymphocytic leukemia

T-PLL · T-cell chronic lymphocytic leukemia

ORPHA:86871