dystonia 32
MONDO:0030486Mondo
Findings
No curated finding names dystonia 32 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Young adult onset
HPO, annotations 2026-09-02
Features
8 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Brain atrophyHPOHP:0012444
- 1 of 1 reported patient
- DysarthriaHPOHP:0001260
- 1 of 1 reported patient
- DysphagiaHPOHP:0002015
- 1 of 1 reported patient
- Laryngeal dystoniaHPOHP:0012049
- 1 of 1 reported patient
- Limb dystoniaHPOHP:0002451
- 1 of 1 reported patient
- Lower limb hyperreflexiaHPOHP:0002395
- 1 of 1 reported patient
- T2 hypointense basal gangliaHPOHP:0012753
- 1 of 1 reported patient
- TorticollisHPOHP:0000473
- 1 of 1 reported patient
Where it sits
Other names
1 name
Resolves to: dystonia 32
- Also called
- DYT32