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

Lissencephaly due to TUBA1A mutation

Familial amyloid polyneuropathy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TUBA1A	(0.63)	TTR

Citations in the biomedical literature:

Lissencephaly due to TUBA1A mutation		Familial amyloid polyneuropathy
	Synonym(s): (no synonyms)		Synonym(s): - TTR amyloid neuropathy - Transthyretin amyloid neuropathy - Transthyretin amyloid polyneuropathy

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Endocrine, nutritional and metabolic diseases -

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

No signs/symptoms info available.