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 ×

Dystonia 16

DYT16 · Early-onset dystonia parkinsonism

ORPHA:210571

Adult-onset dystonia-parkinsonism

Dystonia-parkinsonism, Paisan-Ruiz type · PARK14

ORPHA:199351

Cyanide-induced parkinsonism-dystonia

ORPHA:306692

Dystonia-parkinsonism-hypermanganesemia syndrome

ORPHA:521406

Early-onset generalized limb-onset dystonia

Dystonia musculorum deformans · EOTD

ORPHA:256

Early-onset parkinsonism-intellectual disability syndrome

Laxova-Opitz syndrome · Waisman syndrome

ORPHA:2379

Infantile dystonia-parkinsonism

Dopamine transporter deficiency syndrome · IPD

ORPHA:238455

Progressive supranuclear palsy-predominant parkinsonism syndrome

PSP-p · PSP-parkinsonism

ORPHA:240085

Rapid-onset dystonia-parkinsonism

DYT12 · Dystonia 12

ORPHA:71517

X-linked dystonia-parkinsonism

DYT3 · Lubag

ORPHA:53351

Young-onset Parkinson disease

Early-onset Parkinson disease · YOPD

ORPHA:2828