ODCs

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

PROTEIN INTERACTIONS: 1

16 OMIM references -
4 associated genes
No signs/symptoms info

Spinocerebellar ataxia with axonal neuropathy type 2

Early-onset autosomal dominant Alzheimer disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PIK3R5	(0.56)	APP

Citations in the biomedical literature:

Spinocerebellar ataxia with axonal neuropathy type 2		Early-onset autosomal dominant Alzheimer disease
	Synonym(s): - AOA2 - Ataxia - oculomotor apraxia type 2 - SCAN 2 - SCAR1		Synonym(s): - EOFAD - Early-onset familial autosomal dominant Alzheimer disease - Familial Alzheimer disease

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

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

	Epidemiological data: Class of prevalence: - Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: adult Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 16 OMIM references - No MeSH references

No signs/symptoms info available.