Cytoscape Web
Click node...


1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 OMIM references -
4 associated genes
No signs/symptoms info
APC-related attenuated familial adenomatous polyposis
Autosomal dominant Emery-Dreifuss muscular dystrophy

APC LMNA
SYNE1
SYNE2
TMEM43


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
APC
(0.63)
SYNE1



Citations in the biomedical literature:


APC-related attenuated familial adenomatous polyposis
APC
Autosomal dominant Emery-Dreifuss muscular dystrophy
LMNA SYNE1 SYNE2 TMEM43



APC-related attenuated familial adenomatous polyposis
Autosomal dominant Emery-Dreifuss muscular dystrophy

Synonym(s):
- APC-related AFAP
- APC-related attenuated FAP
- APC-related attenuated familial polyposis coli

Synonym(s):
(no synonyms)

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

Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Diseases of the nervous system -

Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)

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

No signs/symptoms info available.