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"

16 matching diseasesClear search ×

Neonatal compartment syndrome

Neonatal Volkmann ischemic contracture syndrome · Congenital Volkmann ischemic contracture syndrome

ORPHA:641829

Bruck syndrome

Osteogenesis imperfecta-congenital joint contractures syndrome

ORPHA:2771

Congenital cataract-anterior segment dysgenesis syndrome

Congenital cataract-anterior segment mesenchymal dysgenesis syndrome · Congenital cataract-ASD syndrome

ORPHA:162

Congenital Horner syndrome

Congenital Claude-Bernard-Horner syndrome

ORPHA:91413

Congenital long QT syndrome

Congenital LQTS

ORPHA:768

Congenital myasthenic syndrome

CMS

ORPHA:590

Congenital rubella syndrome

Mother-to-child transmission of rubella syndrome · CRS

ORPHA:290

Congenital short QT syndrome

Congenital SQTS

ORPHA:51083

Congenital varicella syndrome

Mother-to-child transmission of varicella syndrome · Antenatal varicella virus infection

ORPHA:291

Congenital vascular bone syndrome

ORPHA:235832

Fetal akinesia-cerebral and retinal hemorrhage syndrome

Lethal congenital contracture syndrome type 5 · LCCS5

ORPHA:363409

Hereditary hyperekplexia

Congenital stiff man syndrome · Familial startle disease

ORPHA:3197

Lethal congenital contracture syndrome

LCCS

ORPHA:294965

Lethal congenital contracture syndrome type 1

Herva disease · LCCS1

ORPHA:1486

Lethal congenital contracture syndrome type 2

LCCS2 · Multiple contracture syndrome, Israeli-Bedouin type

ORPHA:137776

Lethal congenital contracture syndrome type 3

LCCS3

ORPHA:137783