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Muscle filaminopathy
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Myotilin-related myofibrillar myopathy without spheroid body
1 OMIM reference -
1 associated gene
No signs/symptoms info
Muscle filaminopathy
Myotilin-related myofibrillar myopathy without spheroid body

FLNC
(UniProt - OMIM)
 MYOT
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FLNC
(0.79)
MYOT


Citations in the biomedical literature:


Muscle filaminopathy
FLNC
Myotilin-related myofibrillar myopathy without spheroid body
MYOT



Muscle filaminopathy
Myotilin-related myofibrillar myopathy without spheroid body

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Diseases of the nervous system -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
1 OMIM reference -
No MeSH references
No signs/symptoms info available.