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"

4 matching diseasesClear search ×

Fallot complex-intellectual disability-growth delay syndrome

Bindewald-Ulmer-Müller syndrome

ORPHA:3304

Baller-Gerold syndrome

ORPHA:1225

Maxillonasal dysplasia

Binder syndrome · Maxillonasal dysostosis

ORPHA:1248

Postaxial acrofacial dysostosis

Miller syndrome · POADS

ORPHA:246