ODCs

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

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Progressive non-fluent aphasia

Progressive supranuclear palsy - progressive non fluent aphasia


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PSEN1	(0.55)	MAPT

Citations in the biomedical literature:

Progressive non-fluent aphasia		Progressive supranuclear palsy - progressive non fluent aphasia
	Synonym(s): - Agramatic variant of PPA - Agramatic variant of primary progressive aphasia - Non-fluent variant PPA		Synonym(s): - PSP-AOS - PSP-PNFA - Progressive supranuclear palsy - apraxia of speech

	Classification (Orphanet): - 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: 1-9 / 100 000 Average age onset: adulthood Average age of death: - Type of inheritance: multigenic/multifactorial		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: elderly Type of inheritance: sporadic

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

No signs/symptoms info available.