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1 OMIM reference -
1 associated gene
3 signs/symptoms
PROTEIN INTERACTIONS: 2
7 OMIM references -
12 associated genes
No signs/symptoms info
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary nonpolyposis colon cancer

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


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APP
APP
(0.56)
(0.56)
KRAS
TGFBR2



Citations in the biomedical literature:


Hereditary cerebral hemorrhage with amyloidosis, Arctic type
APP
Hereditary nonpolyposis colon cancer
BMPR1A EPCAM KRAS LRRFIP2 MLH1 MLH3
MSH2 MSH6 PIK3CA PMS1 PMS2 TGFBR2



Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary nonpolyposis colon cancer

Synonym(s):
- HCHWA, Arctic type

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

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
(no data available)

Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -

Epidemiological data:
(no data available)
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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type

Very frequent
- Autosomal dominant inheritance
- Psychic / behavioural troubles
- Psychic / psychomotor regression / dementia / intellectual decline



Hereditary nonpolyposis colon cancer

(no data available)