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"

62 matching diseasesClear search ×

Radiation-induced disorder

ORPHA:521132

Radiation-induced plexopathy

ORPHA:521123

Rare disorder due to unbalanced inter-twin blood transfusion

ORPHA:617310

Recurrent hepatitis C virus induced liver disease in liver transplant recipients

ORPHA:90052

Renin-angiotensin-aldosterone system-blocker-induced angioedema

ACEI-related acquired angioedema · Acquired angioedema with normal C1INH

ORPHA:100057

Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome

Rolandic epilepsy exercise-induced dystonia

ORPHA:163727

Scarring in glaucoma filtration surgical procedures

ORPHA:90080

Scedosporiosis

ORPHA:449280

Short stature-advanced bone age-early-onset osteoarthritis syndrome

ORPHA:435804

Spontaneous heparin-induced thrombocytopenia

Spontaneous HIT

ORPHA:699021

Syndrome of reduced sensitivity to thyroid hormone

ORPHA:596426

Vaccine-induced immune thrombotic thrombocytopenia

VITT

ORPHA:699029

Ventilator-induced diaphragmatic dysfunction

VIDD

ORPHA:505395

X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome

ORPHA:482606