Additional Disease Briefs

Parkinson disease 22, autosomal dominant

Also known as: CHCHD2 Parkinson disease, PARK22, Parkinson disease 22, autosomal dominant, Parkinson disease 22, autosomal dominant; PARK22, Parkinson disease caused by mutation in CHCHD2

parkinsonism due to ATP13A2 deficiency

Also known as: CLN12 disease

parkinsonism with dementia of Guadeloupe

parkinsonism with polyneuropathy

parkinsonism-dystonia 3, childhood-onset

parkinsonism-dystonia, infantile

Also known as: IPD, PARKINSONISM-dystonia, infantile, PKDYS, Parkinsonism-dystonia infantile, dopamine transporter deficiency syndrome, infantile Parkinsonism-dystonia, parkinsonism-dystonia, infantile

paroxysmal dyskinesia

Also known as: paroxysmal choreoathetosis, paroxysmal dystonic choreoathetosis

paroxysmal dystonia

paroxysmal extreme pain disorder

Also known as: PEPD, Pexpd, familial rectal pain, familial rectal syndrome, pain, submandibular, ocular, and rectal, with flushing, paroxysmal extreme pain disorder, rectal pain, familial, submandibular, ocular, and rectal pain with flushing