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"

6 matching diseasesClear search ×

Epilepsy of infancy with migrating focal seizures

EIMFS · Malignant migrating partial seizures of infancy

ORPHA:293181

Benign partial epilepsy of infancy with complex partial seizures

ORPHA:166299

Benign partial epilepsy with secondarily generalized seizures in infancy

ORPHA:166302

Epilepsy with generalized tonic-clonic seizures alone

Epilepsy with grand mal seizures on awakening · GTCA

ORPHA:698005

Epilepsy with myoclonic-atonic seizures

Doose syndrome · EMAS

ORPHA:1942

Epilepsy with reading-induced seizures

EwRIS

ORPHA:166433