Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
7 OMIM references -
12 associated genes
No signs/symptoms info
CLOVE syndrome
Hereditary nonpolyposis colon cancer

PIK3CA BMPR1A
EPCAM
KRAS
LRRFIP2
MLH1
MLH3
MSH2
MSH6
PIK3CA
PMS1
PMS2
TGFBR2


COMMON
GENES
PIK3CA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PIK3CA
(0.7)
KRAS



Citations in the biomedical literature:


CLOVE syndrome
PIK3CA
Hereditary nonpolyposis colon cancer
BMPR1A EPCAM KRAS LRRFIP2 MLH1 MLH3
MSH2 MSH6 PMS1 PMS2 TGFBR2



CLOVE syndrome
Hereditary nonpolyposis colon cancer

Synonym(s):
- Congenital lipomatous overgrowth - vascular malformation - epidermal nevi

Synonym(s):
- Familial nonpolyposis colon cancer
- Familial nonpolyposis colorectal cancer
- HNPCC
- Hereditary nonpolyposis colorectal cancer
- Lynch syndrome

Classification (Orphanet):
- Rare circulatory system disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare oncologic disease
- Rare skin disease
Classification (Orphanet):
(no data available)

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

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant

External references:
1 OMIM reference -
No MeSH references
External references:
7 OMIM references -
1 MeSH reference: D003123

No signs/symptoms info available.