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"

3 matching diseasesClear search ×

Systemic capillary leak syndrome

Capillary hyperpermeability syndrome · Capillary leak syndrome

ORPHA:188

Familial articular hypermobility syndrome

Familial joint instability syndrome · Familial joint laxity

ORPHA:2295

Hypermobile Ehlers-Danlos syndrome

EDS-HT · Ehlers-Danlos syndrome hypermobility type

ORPHA:285