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"

9 matching diseasesClear search ×

Self-limited childhood occipital epilepsy

Benign occipital epilepsy

ORPHA:25968

Childhood occipital visual epilepsy

COVE · Idiopathic chilldhood occipital epilepsy-Gastaut type

ORPHA:98816

Myoclonic epilepsy of infancy

Benign myoclonus epilepsy of infancy · Benign myoclonic epilepsy of infancy

ORPHA:86909

Photosensitive occipital lobe epilepsy

POLE

ORPHA:166409

Self-limited epilepsy with autonomic seizures

Benign childhood occipital epilepsy, Panayiotopoulos type · SeLEAS

ORPHA:98815

Self-limited epilepsy with centrotemporal spikes

BRE · Benign epilepsy of childhood with centrotemporal spikes

ORPHA:1945

Self-limited infantile epilepsy

BFIE · BFIS

ORPHA:306

Self-limited neonatal epilepsy

BFNS · Benign familial neonatal convulsions

ORPHA:1949

Self-limited neonatal-infantile epilepsy

SeLFNIE · Benign familial neonatal-infantile seizures

ORPHA:140927