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"

5 matching diseasesClear search ×

Huriez syndrome

Palmoplantar keratoderma-sclerodactyly syndrome · Palmoplantar hyperkeratosis-sclerodactyly syndrome

ORPHA:384

Myosclerosis

Congenital myosclerosis, Löwenthal type

ORPHA:289380

Sclerosteosis

Cortical hyperostosis-syndactyly syndrome

ORPHA:3152

Systemic sclerosis

Progressive systemic sclerosis · Scleroderma

ORPHA:90291

Tuberous sclerosis complex

Bourneville disease · Bourneville syndrome

ORPHA:805