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"

61 matching diseasesClear search ×

Rare hemorrhagic disorder due to a coagulation factors defect

Rare bleeding disorder due to a coagulation factors defect · Rare coagulopathy due to a coagulation factor defect

ORPHA:248315

Rare hemorrhagic disorder due to a constitutional coagulation factors defect

Rare bleeding disorder due to a constitutional coagulation factors defect · Rare coagulopathy due to a constitutional coagulation factors defect

ORPHA:68334

Rare hemorrhagic disorder due to a constitutional platelet anomaly

Rare bleeding disorder due to a constitutional platelet anomaly · Rare bleeding disorder due to a constitutional thrombopathy and/or thrombocytopenia

ORPHA:71202

Rare hemorrhagic disorder due to a constitutional thrombocytopenia

Rare hemorrhagic disorder due to a quantitative platelet defect · Rare bleeding disorder due to a quantitative platelet defect

ORPHA:275729

Rare hemorrhagic disorder due to a platelet anomaly

Rare bleeding disorder due to a platelet anomaly · Rare bleeding disorder due to a thrombopathy and/or thrombocytopenia

ORPHA:248326

Rare hemorrhagic disorder due to a qualitative platelet defect

Rare bleeding disorder due to a constitutional thrombopathy · Rare coagulopathy due to a constitutional thrombopathy

ORPHA:275736

Rare hemorrhagic disorder due to an acquired coagulation factor defect

Rare bleeding disorder due to an acquired coagulation factor defect · Rare coagulopathy due to an acquired coagulation factor defect

ORPHA:166775

Rare hemorrhagic disorder due to an acquired platelet anomaly

Rare bleeding disorder due to an acquired platelet anomaly · Rare bleeding disorder due to an acquired thrombopathy and/or thrombocytopenia

ORPHA:248347

Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome

TANGO2-related metabolic encephalopathy-arrhythmia syndrome

ORPHA:480864

Seborrhea-like dermatitis with psoriasiform elements

ORPHA:168606

Syndromic congenital sodium diarrhea

Syndromic congenital tufting enteropathy

ORPHA:563708

Venezuelan hemorrhagic fever

Guanarito hemorrhagic fever

ORPHA:319234

Viral hemorrhagic fever

ORPHA:341