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APC-related attenuated familial adenomatous polyposis
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Autosomal recessive myogenic arthrogryposis multiplex congenita
1 associated gene
No signs/symptoms info
APC-related attenuated familial adenomatous polyposis
Autosomal recessive myogenic arthrogryposis multiplex congenita

APC
(UniProt - OMIM)
 SYNE1
(UniProt - OMIM)

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 recessive myogenic arthrogryposis multiplex congenita
SYNE1



APC-related attenuated familial adenomatous polyposis
Autosomal recessive myogenic arthrogryposis multiplex congenita

Synonym(s):
- APC-related AFAP
- APC-related attenuated FAP
- APC-related attenuated familial polyposis coli
Synonym(s):
- Autosomal recessive myogenic AMC
- SYNE1-related AMC
- SYNE1-related arthrogryposis multiplex congenita
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
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:
No OMIM references
No MeSH references
No signs/symptoms info available.