ODCs

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

PROTEIN INTERACTIONS: 1

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

Inherited congenital spastic tetraplegia

Spinocerebellar ataxia type 1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ADD3	(0.63)	ATXN1

Citations in the biomedical literature:

Inherited congenital spastic tetraplegia		Spinocerebellar ataxia type 1
	Synonym(s): - Inherited congenital spastic quadriplegia		Synonym(s): - SCA1

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: - 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.