Rare Disease Library

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"

5 matching diseasesClear search ×

Myoclonic epilepsy in non-progressive encephalopathies

Myoclonus epilepsy in non-progressive encephalopathies · Myoclonic status in non-progressive encephalopathies

ORPHA:86913

Early myoclonic encephalopathy

Early myoclonic encephalopathy with suppression-bursts

ORPHA:1935

Early-onset progressive encephalopathy with migrant continuous myoclonus

ORPHA:1943

Progressive encephalomyelitis with rigidity and myoclonus

PERM

ORPHA:438266

Progressive myoclonic epilepsy

PME · Progressive myoclonus epilepsy

ORPHA:98261