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Spinocerebellar ataxia type 10
1 OMIM reference -
1 associated gene
16 connected diseases
No signs/symptoms info
Disease Type of connection
Joubert syndrome with renal defect
Giant cell glioblastoma
Adult-onset distal myopathy due to VCP mutation
Amyotrophic lateral sclerosis
Apolipoprotein A-I deficiency
Behavioral variant of frontotemporal dementia
Combined oxidative phosphorylation defect type 2
Fibronectin glomerulopathy
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Osteogenesis imperfecta type 3
Progressive non-fluent aphasia
Pseudohypoaldosteronism type 2E
Semantic dementia
Spastic paraplegia - Paget disease of bone
Tangier disease
- SCA10

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
ATXN10 Q9UBB4611150
No signs/symptoms info available.