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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
4 signs/symptoms
Gardner syndrome
Sebocystomatosis

APC KRT17


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Gardner syndrome
APC
Sebocystomatosis
KRT17



Gardner syndrome
Sebocystomatosis

Synonym(s):
(no synonyms)

Synonym(s):
- Steatocystoma multiplex

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
- Rare skin 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:
1 OMIM reference -
1 MeSH reference: D005736
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


Gardner syndrome

(no data available)