spinocerebellar ataxia type 32
MONDO:0013486Mondo
Findings
No curated finding names spinocerebellar ataxia type 32 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Spinocerebellar ataxia type 32 (SCA32) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by ataxia, cognitive impairment and azoospermia in males.
Definition from the Mondo Disease Ontology (MONDO:0013486), read 2026-09-29. CC BY 4.0.
Features
6 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.
- AzoospermiaHPOHP:0000027
- Frequent (30% to 79% of cases)
- Cerebellar atrophyHPOHP:0001272
- Frequent (30% to 79% of cases)
- Cognitive impairmentHPOHP:0100543
- Frequent (30% to 79% of cases)
- Male infertilityHPOHP:0003251
- Frequent (30% to 79% of cases)
- Progressive cerebellar ataxiaHPOHP:0002073
- Frequent (30% to 79% of cases)
- Testicular atrophyHPOHP:0000029
- Frequent (30% to 79% of cases)
Where it sits
Other names
2 names
Resolves to: spinocerebellar ataxia type 32
- Also called
- cerebellar ataxia with azoospermia and intellectual disabilitySCA32