ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

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

Intellectual deficit, X-linked, Turner type

MUTYH-related attenuated familial adenomatous polyposis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HUWE1	(0.7)	MUTYH

Citations in the biomedical literature:

Intellectual deficit, X-linked, Turner type		MUTYH-related attenuated familial adenomatous polyposis
	Synonym(s): (no synonyms)		Synonym(s): - MUTYH-related AFAP - MUTYH-related attenuated FAP - MUTYH-related attenuated familial polyposis coli

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

	Classification (ICD10): (no data available)		Classification (ICD10): - Neoplasms -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: x-linked dominant		Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - 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.