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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"
Familial adult myoclonic epilepsy
ADCME · Autosomal dominant cortical myoclonus and epilepsy
Epilepsy with myoclonic-atonic seizures
Doose syndrome · EMAS
Familial cortical myoclonus
Familial infantile myoclonic epilepsy
FIME · Familial infantile myoclonus epilepsy
Familial partial epilepsy