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 ×

Paroxysmal kinesigenic dyskinesia

Familial PKD · Familial paroxysmal kinesigenic dyskinesia

ORPHA:98809

Familial dyskinesia and facial myokymia

FDFM

ORPHA:324588

Familial Mediterranean fever

Benign paroxysmal peritonitis · Benign recurrent polyserositis

ORPHA:342

Familial paroxysmal ataxia

Episodic ataxia type 2

ORPHA:97

Infantile convulsions and choreoathetosis

ICCA syndrome · Paroxysmal kinesigenic dyskinesia and infantile convulsions

ORPHA:31709

Paroxysmal dyskinesia

Paroxysmal choreoathetosis · Paroxysmal dystonic choreoathetosis

ORPHA:1431

Paroxysmal exertion-induced dyskinesia

DYT18 · Dystonia 18

ORPHA:98811

Paroxysmal hypnogenic dyskinesia

Nocturnal paroxysmal dystonia · Paroxysmal hypnagogic dyskinesia

ORPHA:98812

Paroxysmal non-kinesigenic dyskinesia

Paroxystic non-kinesigenic choreoathetosis

ORPHA:98810