ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Familial advanced sleep-phase syndrome

Progressive supranuclear palsy - progressive non fluent aphasia

CSNK1D	(UniProt - OMIM)		MAPT	(UniProt - OMIM)
PER2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CSNK1D	(0.59)	MAPT

Citations in the biomedical literature:

Familial advanced sleep-phase syndrome		Progressive supranuclear palsy - progressive non fluent aphasia
	Synonym(s): - FASPS		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: - Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adulthood Average age of death: elderly Type of inheritance: sporadic

	External references: 2 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

No signs/symptoms info available.