neurodegenerative disorder with cerebellar and caudate atrophy
MONDO:0981024Mondo
Findings
No curated finding names neurodegenerative disorder with cerebellar and caudate atrophy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
86 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.
- Action tremorHPOHP:0002345
- 1 of 1 reported patient
- Aggressive behaviorHPOHP:0000718
- 1 of 1 reported patient
- ApraxiaHPOHP:0002186
- 1 of 1 reported patient
- AreflexiaHPOHP:0001284
- 5 of 5 reported patients
- AtaxiaHPOHP:0001251
- 6 of 6 reported patients
- Attention deficit hyperactivity disorderHPOHP:0007018
- 1 of 1 reported patient
- Atypical behaviorHPOHP:0000708
- 2 of 2 reported patients
- BradykinesiaHPOHP:0002067
- 1 of 1 reported patient
- Breech presentationHPOHP:0001623
- 1 of 1 reported patient
- Caesarean sectionHPOHP:0011410
- 1 of 1 reported patient
- CataractHPOHP:0000518
- 1 of 1 reported patient
- Caudate atrophyHPOHP:0002340
- 11 of 11 reported patients
Show the remaining 74
- Cerebellar atrophyHPOHP:0001272
- 11 of 11 reported patients
- Cerebral visual impairmentHPOHP:0100704
- 1 of 1 reported patient
- ChoreaHPOHP:0002072
- 1 of 1 reported patient
- Clinodactyly of the 5th fingerHPOHP:0004209
- 1 of 1 reported patient
- ClumsinessHPOHP:0002312
- 2 of 2 reported patients
- Cognitive impairmentHPOHP:0100543
- 1 of 1 reported patient
Where it sits
- A kind of