ODCs

Cytoscape Web

Click node...

Sebocystomatosis

1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

Gardner syndrome

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

Sebocystomatosis

Gardner syndrome

(UniProt - OMIM)

(UniProt - OMIM)


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

Citations in the biomedical literature:

Sebocystomatosis		Gardner syndrome
	Synonym(s): - Steatocystoma multiplex		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: adolescence / young 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 - 1 MeSH reference: D005736

Sebocystomatosis
	Very frequent - Adenoma sebaceum - Autosomal dominant inheritance - Skin tumors / lumps / epidermal cysts Occasional - Urinary / renal lithiasis / kidney stones / nephritic colic
Gardner syndrome
(no data available)