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1 OMIM reference -
2 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 1
2 associated genes
No signs/symptoms info
Familial gastric cancer
Craniopharyngioma

CDH1 BRAF
MUTYH CTNNB1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
CDH1
(0.97)
CTNNB1



Citations in the biomedical literature:


Familial gastric cancer
CDH1 MUTYH
Craniopharyngioma
BRAF CTNNB1



Familial gastric cancer
Craniopharyngioma

Synonym(s):
- Familial stomach cancer

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare endocrine disease
- Rare neurologic disease
- Rare oncologic disease

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: variable
Average age of death: -
Type of inheritance: sporadic

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
1 MeSH reference: D003397

No signs/symptoms info available.