ODCs

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1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Progressive supranuclear palsy - corticobasal syndrome

Distal hereditary motor neuropathy type 7

MAPT	(UniProt - OMIM)		DCTN1	(UniProt - OMIM)
			SLC5A7	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MAPT	(0.75)	DCTN1

Citations in the biomedical literature:

Progressive supranuclear palsy - corticobasal syndrome		Distal hereditary motor neuropathy type 7
	Synonym(s): - PSP-CBS - PSP-corticobasal syndrome		Synonym(s): - Distal spinal muscular atrophy with vocal cord paralysis - dHMN7

	Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - 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 / 1 000 000 Average age onset: adulthood Average age of death: elderly Type of inheritance: sporadic		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.