ODCs

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

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Lissencephaly due to TUBA1A mutation

Machado-Joseph disease type 1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TUBA1A	(0.56)	ATXN3

Citations in the biomedical literature:

Lissencephaly due to TUBA1A mutation		Machado-Joseph disease type 1
	Synonym(s): (no synonyms)		Synonym(s): - SCA3, Joseph type

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

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

	Epidemiological data: (no data available)		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		External references: No OMIM references No MeSH references

No signs/symptoms info available.