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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"
Hereditary motor and sensory neuropathy with acrodystrophy
AR-CMT2 with acrodystrophy · Autosomal recessive Charcot-Marie-Tooth type 2 with acrodystrophy
Complex regional pain syndrome type 1
Algodystrophy · Reflex sympathetic dystrophy
Laminopathy with lipodystrophy