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Familial adenomatous polyposis due to 5q22.2 microdeletion

1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Sebocystomatosis

1 OMIM reference -
1 associated gene
4 signs/symptoms

Familial adenomatous polyposis due to 5q22.2 microdeletion

Sebocystomatosis

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	APC	(0.63)	KRT17

Citations in the biomedical literature:

Familial adenomatous polyposis due to 5q22.2 microdeletion		Sebocystomatosis
	Synonym(s): - Colorectal adenomatous polyposis due to monosomy 5q22.2 - FAP due to monosomy 5q22.2 - Familial adenomatous polyposis due to del(5)(q22.2) - Familial adenomatous polyposis due to monosomy 5q22.2 - Familial polyposis coli due to monosomy 5q22.2		Synonym(s): - Steatocystoma multiplex

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare genetic disease - Rare skin disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the skin and subcutaneous tissue -

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

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

Sebocystomatosis
	Very frequent - Adenoma sebaceum - Autosomal dominant inheritance - Skin tumors / lumps / epidermal cysts Occasional - Urinary / renal lithiasis / kidney stones / nephritic colic
Familial adenomatous polyposis due to 5q22.2 microdeletion
(no data available)