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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"
Sialidosis type 1
Cherry-red spot-myoclonus syndrome · Lipomucopolysaccharidosis
Action myoclonus-renal failure syndrome
AMRF · Progressive myoclonus epilepsy type 4
Myoclonus-dystonia syndrome
Alcohol-responsive dystonia · Hereditary essential myoclonus
Opsoclonus-myoclonus syndrome
Ataxo-opso-myoclonus syndrome · Dancing eye syndrome