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"

8 matching diseasesClear search ×

Genetic epilepsy with febrile seizure plus

GEFS+ · Generalized epilepsy with febrile seizures plus

ORPHA:36387

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

Familial mesial temporal lobe epilepsy with febrile seizures

ORPHA:165805

OBSOLETE: Generalized epilepsy and praxis-induced seizures

ORPHA:99649

Self-limited epilepsy with autonomic seizures

Benign childhood occipital epilepsy, Panayiotopoulos type · SeLEAS

ORPHA:98815