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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"
ABeta2M amyloidosis
Beta2-microglobulinic amyloidosis
Amyloidosis
Variant ABeta2M amyloidosis
Autosomal dominant beta2-microglobulinic amyloidosis
Wild type ABeta2M amyloidosis
ABeta2Mwt amyloidosis · Dialysis-related amyloidosis