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

LMNA
(UniProt - OMIM)
 APC
(UniProt - OMIM)
SYNE1
(UniProt - OMIM)
SYNE2
(UniProt - OMIM)
TMEM43
(UniProt - OMIM)

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


Citations in the biomedical literature:


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



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

Synonym(s):
(no synonyms)

Synonym(s):
- APC-related AFAP
- APC-related attenuated FAP
- APC-related attenuated familial polyposis coli
Classification (Orphanet):
- Rare cardiac disease
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
External references:
4 OMIM references -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.