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

PROTEIN INTERACTIONS: 1

Semantic dementia

6 associated genes
No signs/symptoms info

CLN6 disease

Semantic dementia

CLN6	(UniProt - OMIM)		C9ORF72	(UniProt - OMIM)
			CHMP2B	(UniProt - OMIM)
			GRN	(UniProt - OMIM)
			MAPT	(UniProt - OMIM)
			PSEN1	(UniProt - OMIM)
			VCP	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CLN6	(0.63)	VCP

Citations in the biomedical literature:

CLN6 disease		Semantic dementia
	Synonym(s): (no synonyms)		Synonym(s): - Semantic primary progressive aphasia - Semantic variant PPA

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: - Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		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.