spinocerebellar ataxia 51
MONDO:0975800Mondo
Findings
No curated finding names spinocerebellar ataxia 51 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
- Onset and course
- Middle age onset · Childhood onset · Late young adult onset
HPO, annotations 2026-09-02
Features
11 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.
- AtaxiaHPOHP:0001251
- 5 of 5 reported patients
- DysarthriaHPOHP:0001260
- 5 of 5 reported patients
- Gait ataxiaHPOHP:0002066
- 5 of 5 reported patients
- Abnormal pyramidal signHPOHP:0007256
- 1 of 5 reported patients
- Cognitive impairmentHPOHP:0100543
- 1 of 5 reported patients
- DysphagiaHPOHP:0002015
- 1 of 5 reported patients
- MyoclonusHPOHP:0001336
- 1 of 5 reported patients
- NystagmusHPOHP:0000639
- 1 of 5 reported patients
- PtosisHPOHP:0000508
- 1 of 5 reported patients
- Slow saccadic eye movementsHPOHP:0000514
- 1 of 5 reported patients
- Somatic sensory dysfunctionHPOHP:0003474
- 0 of 5 reported patients
Where it sits
- A kind of