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 ×

Progressive supranuclear palsy-predominant parkinsonism syndrome

PSP-p · PSP-parkinsonism

ORPHA:240085

Adult-onset dystonia-parkinsonism

Dystonia-parkinsonism, Paisan-Ruiz type · PARK14

ORPHA:199351

ATP13A2-related parkinsonism

ORPHA:514980

Atypical juvenile parkinsonism

ORPHA:391411

Caribbean parkinsonism

Atypical parkinsonism in the Caribbean

ORPHA:97355

Dystonia 16

DYT16 · Early-onset dystonia parkinsonism

ORPHA:210571

Infantile dystonia-parkinsonism

Dopamine transporter deficiency syndrome · IPD

ORPHA:238455

Multiple system atrophy, parkinsonian type

MSA, parkinsonian type · MSA-p

ORPHA:98933

Parkinsonism with polyneuropathy

ORPHA:611237

Postencephalitic parkinsonism

ORPHA:97349

Rapid-onset dystonia-parkinsonism

DYT12 · Dystonia 12

ORPHA:71517

X-linked dystonia-parkinsonism

DYT3 · Lubag

ORPHA:53351