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 ×

Qualitative or quantitative defects of dysferlin

Dysferlinopathy

ORPHA:207073

Desminopathy

Desmin-related myofibrillar myopathy

ORPHA:98909

Qualitative or quantitative defects of dystrophin

Dystrophinopathy

ORPHA:207085