ODCs

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

PROTEIN INTERACTIONS: 1

3 OMIM references -
1 associated gene
No signs/symptoms info

Autosomal recessive centronuclear myopathy

Classical progressive supranuclear palsy

BIN1	(UniProt - OMIM)		MAPT	(UniProt - OMIM)
TTN	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	BIN1	(0.7)	MAPT

Citations in the biomedical literature:

Autosomal recessive centronuclear myopathy		Classical progressive supranuclear palsy
	Synonym(s): - AR-CNM		Synonym(s): - Classical PSP - Richardson syndrome - Steele-Richardson-Olszewski disease

	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: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: adulthood Average age of death: elderly Type of inheritance: sporadic

	External references: 1 OMIM reference - No MeSH references		External references: 3 OMIM references - No MeSH references

No signs/symptoms info available.