ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Progressive supranuclear palsy - corticobasal syndrome

Autosomal recessive systemic lupus erythematosus

MAPT	(UniProt - OMIM)		DNASE1L3	(UniProt - OMIM)
			PRKCD	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MAPT	(0.63)	PRKCD

Citations in the biomedical literature:

Progressive supranuclear palsy - corticobasal syndrome		Autosomal recessive systemic lupus erythematosus
	Synonym(s): - PSP-CBS - PSP-corticobasal syndrome		Synonym(s): - Autosomal recessive SLE - Familial SLE - Familial systemic lupus erythematosus

	Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adulthood Average age of death: elderly Type of inheritance: sporadic		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: childhood Average age of death: no data available Type of inheritance: autosomal recessive

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

No signs/symptoms info available.