ODCs

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

PROTEIN INTERACTIONS: 1

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

Spinocerebellar ataxia type 6

Synpolydactyly type 2


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CACNA1A	(0.63)	FBLN1

Citations in the biomedical literature:

Spinocerebellar ataxia type 6		Synpolydactyly type 2
	Synonym(s): - SCA6		Synonym(s): - SD2, Debeer type - SD2b - SPD, Debeer type - SPD2 - Synpolydactyly, Debeer type

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

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

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

No signs/symptoms info available.