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Autosomal recessive myogenic arthrogryposis multiplex congenita
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial adenomatous polyposis due to 5q22.2 microdeletion
1 associated gene
No signs/symptoms info
Autosomal recessive myogenic arthrogryposis multiplex congenita
Familial adenomatous polyposis due to 5q22.2 microdeletion

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

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


Citations in the biomedical literature:


Autosomal recessive myogenic arthrogryposis multiplex congenita
SYNE1
Familial adenomatous polyposis due to 5q22.2 microdeletion
APC



Autosomal recessive myogenic arthrogryposis multiplex congenita
Familial adenomatous polyposis due to 5q22.2 microdeletion

Synonym(s):
- Autosomal recessive myogenic AMC
- SYNE1-related AMC
- SYNE1-related arthrogryposis multiplex congenita
Synonym(s):
- Colorectal adenomatous polyposis due to monosomy 5q22.2
- FAP due to monosomy 5q22.2
- Familial adenomatous polyposis due to del(5)(q22.2)
- Familial adenomatous polyposis due to monosomy 5q22.2
- Familial polyposis coli due to monosomy 5q22.2
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare gastroenterologic disease
- Rare genetic disease
- Rare oncologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.