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"

13 matching diseasesClear search ×

Von Willebrand disease

Hereditary von Willebrand disease · Hereditary pseudohaemophilia

ORPHA:903

Acquired von Willebrand syndrome

Acquired von Willebrand disease

ORPHA:99147

Genetic cystic renal disease

Hereditary cystic renal disease

ORPHA:93587

Hereditary late-onset Parkinson disease

Autosomal dominant late-onset Parkinson disease · LOPD

ORPHA:411602

Hereditary progressive cardiac conduction defect

Hereditary Lenègre disease · Hereditary Lev disease

ORPHA:871

Pseudo-von Willebrand disease

PT-VWD · Pseudo-von Willebrand disease type 2B

ORPHA:52530

Von Willebrand disease type 1

ORPHA:166078

Von Willebrand disease type 2

ORPHA:166081

Von Willebrand disease type 2A

ORPHA:166084

Von Willebrand disease type 2B

ORPHA:166087

Von Willebrand disease type 2M

ORPHA:166090

Von Willebrand disease type 2N

ORPHA:166093

Von Willebrand disease type 3

ORPHA:166096