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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"
Bethlem muscular dystrophy
Bethlem myopathy · LGMD R22 collagen 6-related dystrophy
Collagen VI-related congenital muscular dystrophy
COL6-RD
Congenital muscular dystrophy, Fukuyama type
FCMD · Fukuyama congenital muscular dystrophy
FLNA-related X-linked myxomatous valvular dysplasia
Filamin A-related X-linked myxomatous valvular dysplasia · FLNA-related valvular dystrophy
Intermediate collagen VI-related muscular dystrophy
Intermediate COL6-RD