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"

2 matching diseasesClear search ×

Collagen VI-related congenital muscular dystrophy

COL6-RD

ORPHA:646098

Intermediate collagen VI-related muscular dystrophy

Intermediate COL6-RD

ORPHA:646113