ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Spinocerebellar ataxia with axonal neuropathy type 2

Transthyretin-related familial amyloid cardiomyopathy

PIK3R5	(UniProt - OMIM)		TTR	(UniProt - OMIM)
SETX	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PIK3R5	(0.63)	TTR

Citations in the biomedical literature:

Spinocerebellar ataxia with axonal neuropathy type 2		Transthyretin-related familial amyloid cardiomyopathy
	Synonym(s): - AOA2 - Ataxia - oculomotor apraxia type 2 - SCAN 2 - SCAR1		Synonym(s): - ATTR cardiomyopathy - TTR-related amyloid cardiomyopathy - TTR-related cardiac amyloidosis - Transthyretin amyloid cardiopathy

	Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare cardiac disease - Rare genetic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

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

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.