ODCs

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

PROTEIN INTERACTIONS: 1

6 associated genes
No signs/symptoms info

Familial paroxysmal ataxia

Semantic dementia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CACNA1A	(0.68)	GRN

Citations in the biomedical literature:

Familial paroxysmal ataxia		Semantic dementia
	Synonym(s): - Episodic ataxia type 2		Synonym(s): - Semantic primary progressive aphasia - Semantic variant PPA

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - 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: unknown Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: multigenic/multifactorial

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

No signs/symptoms info available.