ODCs

Click node...

1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 3

3 OMIM references -
3 associated genes
No signs/symptoms info

Spinocerebellar ataxia type 26

Frontotemporal dementia with motor neuron disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	EEF2 SCA26 SCA26	(0.63) (0.63) (0.63)	TARDBP FUS TARDBP

Citations in the biomedical literature:

Spinocerebellar ataxia type 26		Frontotemporal dementia with motor neuron disease
	Synonym(s): - SCA26		Synonym(s): - FTD-ALS - FTD-MND - Frontotemporal dementia with amyotrophic lateral sclerosis

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): (no data available)

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: unknown Average age onset: adulthood Average age of death: adult Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C537203		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.