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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"
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia
ALSP · Autosomal dominant leukoencephalopathy with neuroaxonal spheroids
Familial progressive hyperpigmentation
Melanosis diffusa congenita · Melanosis universalis hereditaria
Progressive familial intrahepatic cholestasis
PFIC