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"

11 matching diseasesClear search ×

Self-limited infantile epilepsy

BFIE · BFIS

ORPHA:306

Benign hereditary chorea

BHC · Benign familial chorea

ORPHA:1429

Benign idiopathic neonatal seizures

BINS · Benign nonfamilial neonatal seizures

ORPHA:64545

Benign non-familial infantile seizures

ORPHA:166295

Benign partial epilepsy of infancy with complex partial seizures

ORPHA:166299

Benign partial infantile seizures

ORPHA:166311

Familial infantile bilateral striatal necrosis

Familial IBSN · Familial infantile striatonigral degeneration

ORPHA:225154

Familial infantile myoclonic epilepsy

FIME · Familial infantile myoclonus epilepsy

ORPHA:352582

Self-limited neonatal epilepsy

BFNS · Benign familial neonatal convulsions

ORPHA:1949

Self-limited neonatal-infantile epilepsy

SeLFNIE · Benign familial neonatal-infantile seizures

ORPHA:140927

X-linked acrogigantism

Hereditary infantile gigantism · Hereditary pituitary hyperplasia

ORPHA:300373