ODCs

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

PROTEIN INTERACTIONS: 1

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

APC-related attenuated familial adenomatous polyposis

Commissural facial cleft

APC	(UniProt - OMIM)		PTCH2	(UniProt - OMIM)
			SPECC1L	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	APC	(0.63)	SPECC1L

Citations in the biomedical literature:

APC-related attenuated familial adenomatous polyposis		Commissural facial cleft
	Synonym(s): - APC-related AFAP - APC-related attenuated FAP - APC-related attenuated familial polyposis coli		Synonym(s): - Macrostomia

	Classification (Orphanet): - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare maxillo-facial surgical disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

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

No signs/symptoms info available.