ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

MUTYH-related attenuated familial adenomatous polyposis

Autosomal dominant Charcot-Marie-Tooth disease type 2P


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MUTYH	(0.73)	LRSAM1

Citations in the biomedical literature:

MUTYH-related attenuated familial adenomatous polyposis		Autosomal dominant Charcot-Marie-Tooth disease type 2P
	Synonym(s): - MUTYH-related AFAP - MUTYH-related attenuated FAP - MUTYH-related attenuated familial polyposis coli		Synonym(s): - CMT2P

	Classification (Orphanet): - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: adolescence / young Average age of death: no data available Type of inheritance: autosomal dominant

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

No signs/symptoms info available.