ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Spinocerebellar ataxia type 7

Synaptic congenital myasthenic syndromes

ATXN7	(UniProt - OMIM)		COLQ	(UniProt - OMIM)
			LAMB2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ATXN7	(0.63)	LAMB2

Citations in the biomedical literature:

Spinocerebellar ataxia type 7		Synaptic congenital myasthenic syndromes
	Synonym(s): - Autosomal dominant spinocerebellar ataxia type 7 - Cerebellar syndrome - pigmentary maculopathy - SCA7		Synonym(s): (no synonyms)

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	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.