ODCs

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

PROTEIN INTERACTIONS: 2

1 associated gene
No signs/symptoms info

Progressive non-fluent aphasia

Hyperlipidemia type 3


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MAPT PSEN1	(0.87) (0.63)	APOE APOE

Citations in the biomedical literature:

Progressive non-fluent aphasia		Hyperlipidemia type 3
	Synonym(s): - Agramatic variant of PPA - Agramatic variant of primary progressive aphasia - Non-fluent variant PPA		Synonym(s): - Broad-betalipoproteinemia - Dyslipidemia type 3 - Familial dysbetalipoproteinemia - Familial hyperlipoproteinemia type 3 - HLP type 3 - Hyperlipoproteinemia type 3 - Remnant disease

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

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: - Type of inheritance: multigenic/multifactorial		Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: variable Average age of death: normal Type of inheritance: multigenic/multifactorial

	External references: 1 OMIM reference - 1 MeSH reference: D057178		External references: No OMIM references 1 MeSH reference: D006952

No signs/symptoms info available.