All patient-facing tools are free · No login required to browse
All access tools are free for patients and caregivers
All community tools are free for patients and caregivers
7 Patents Filed · HIPAA-Aligned · Free for Patients · Westwood, MA
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"
Myofibrillar myopathy
MFM
BAG3-related myofibrillar myopathy
MFM6 · Myofibrillar myopathy type 6
Hereditary myopathy with early respiratory failure
MFM-titinopathy · Hereditary inclusion body myopathy with early respiratory failure
HSPB8-related autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome
MFM13 · Myofibrillar myopathy-rimmed vacuoles type 13
Muscle filaminopathy
FLNC-associated myofibrillar myopathy · Filamin C-related filaminopathy