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"

10 matching diseasesClear search ×

Immune thrombocytopenia

ITP · Immune thrombocytopenic purpura

ORPHA:3002

Autoimmune heparin-induced thrombocytopenia

Autoimmune HIT · aHIT

ORPHA:698945

Autoimmune thrombocytopenia

ORPHA:71203

Classic heparin-induced thrombocytopenia

Classic heparin-associated thrombocytopenia · Classic HAT

ORPHA:3325

Congenital thrombotic thrombocytopenic purpura

Congenital ADAMTS-13 deficiency · Congenital TTP

ORPHA:93583

Evans syndrome

Autoimmune hemolytic anemia and autoimmune thrombocytopenia · Immune pancytopenia

ORPHA:1959

Fetal and neonatal alloimmune thrombocytopenia

FNAIT · NAIT

ORPHA:853

Immune-mediated thrombotic thrombocytopenic purpura

Acquired thrombotic thrombocytopenic purpura · Acquired TTP

ORPHA:93585

Thrombotic thrombocytopenic purpura

Moschcowitz disease · TTP

ORPHA:54057

Vaccine-induced immune thrombotic thrombocytopenia

VITT

ORPHA:699029