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"

7 matching diseasesClear search ×

Self-limited epilepsy with autonomic seizures

Benign childhood occipital epilepsy, Panayiotopoulos type · SeLEAS

ORPHA:98815

Childhood absence epilepsy

Pyknolepsy

ORPHA:64280

Childhood occipital visual epilepsy

COVE · Idiopathic chilldhood occipital epilepsy-Gastaut type

ORPHA:98816

Childhood-onset epilepsy syndrome

ORPHA:98259

Epilepsy with myoclonic-atonic seizures

Doose syndrome · EMAS

ORPHA:1942

Self-limited childhood occipital epilepsy

Benign occipital epilepsy

ORPHA:25968

Self-limited epilepsy with centrotemporal spikes

BRE · Benign epilepsy of childhood with centrotemporal spikes

ORPHA:1945