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 ×

Transient myeloproliferative syndrome

TMD · Transient abnormal myelopoiesis

ORPHA:420611

Alpha-heavy chain disease

Alpha-HCD · IPSID

ORPHA:100025

Chronic myeloproliferative disease, unclassifiable

CMPD-U · Undifferentiated myeloproliferative disease

ORPHA:86830

Myelodysplastic/myeloproliferative disease

MDS · Myelodysplastic syndromes

ORPHA:98275

Myeloid/lymphoid neoplasm associated with FGFR1 rearrangement

8p11 myeloproliferative syndrome · Stem cell leukemia/lymphoma

ORPHA:168953

Myeloproliferative neoplasm

MPD · MPN

ORPHA:98274

Post-transplant lymphoproliferative disease

PTLD

ORPHA:70568

Unclassified myelodysplastic/myeloproliferative disease

MDS · Myelodysplastic syndromes

ORPHA:98825

X-linked lymphoproliferative disease

Duncan disease · Purtilo syndrome

ORPHA:2442