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"

13 matching diseasesClear search ×

Myoclonic dystonia 15

DYT15 · Myoclonus-dystonia type 15

ORPHA:210566

Myoclonus-dystonia syndrome

Alcohol-responsive dystonia · Hereditary essential myoclonus

ORPHA:36899

Myotonic dystrophy type 3

ORPHA:54238

Primary dystonia, DYT13 type

DYT13 · Primary dystonia with mixed phenotype

ORPHA:98807

Primary dystonia, DYT17 type

ORPHA:370103

Primary dystonia, DYT2 type

DYT2

ORPHA:99657

Primary dystonia, DYT21 type

DYT21

ORPHA:306734

Primary dystonia, DYT27 type

ORPHA:464440

Primary dystonia, DYT4 type

DYT4 · Hereditary whispering dysphonia

ORPHA:98805

Primary dystonia, DYT6 type

DYT6 · Generalized cervical and upper-limb-onset dystonia

ORPHA:98806

Progressive myoclonic epilepsy with dystonia

PMED · Progressive myoclonus epilepsy with dystonia

ORPHA:352596

Proximal myotonic myopathy

Myotonic dystrophy type 2 · Proximal myotonic dystrophy

ORPHA:606

Steinert myotonic dystrophy

Myotonic dystrophy type 1 · Steinert disease

ORPHA:273