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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"
Laminin subunit alpha 2-related limb-girdle muscular dystrophy R23
Laminin subunit alpha 2-related late-onset muscular dystrophy · Laminin subunit alpha 2-related LGMD R23
Alpha-sarcoglycan-related limb-girdle muscular dystrophy R3
Alpha-sarcoglycanopathy · LGMD2D
Laminin subunit alpha 2-related congenital muscular dystrophy
CMD1A · Congenital muscular dystrophy due to laminin alpha2 deficiency
Laminin subunit alpha 2-related muscular dystrophy
LAMA2-related muscular dystrophy · Qualitative or quantitative defects of merosin