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"

12 matching diseasesClear search ×

Self-limited neonatal epilepsy

BFNS · Benign familial neonatal convulsions

ORPHA:1949

Benign hereditary chorea

BHC · Benign familial chorea

ORPHA:1429

Benign idiopathic neonatal seizures

BINS · Benign nonfamilial neonatal seizures

ORPHA:64545

Familial adult myoclonic epilepsy

ADCME · Autosomal dominant cortical myoclonus and epilepsy

ORPHA:86814

Familial mesial temporal lobe epilepsy

FLTLE

ORPHA:163717

Familial partial epilepsy

ORPHA:309

Familial temporal lobe epilepsy

ORPHA:98819

OBSOLETE: Neonatal epilepsy syndrome

ORPHA:98257

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

Self-limited infantile epilepsy

BFIE · BFIS

ORPHA:306

Self-limited neonatal-infantile epilepsy

SeLFNIE · Benign familial neonatal-infantile seizures

ORPHA:140927