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 ×

Myeloid/lymphoid neoplasm associated with JAK2 rearrangement

Myeloid/lymphoid neoplasms with PCM1-JAK2

ORPHA:589542

Acute lymphoblastic leukemia

ALL · Acute lymphoblastic leukemia/lymphoma

ORPHA:513

Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement

8p11 myeloproliferative syndrome · Stem cell leukemia/lymphoma

ORPHA:168953

Myeloid/lymphoid neoplasm associated with PDGFRA rearrangement

ORPHA:168947

Myeloid/lymphoid neoplasm associated with PDGFRB rearrangement

ORPHA:168950

Myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2

ORPHA:168943