Cytoscape Web
Click node...

Myotilin-related myofibrillar myopathy without spheroid body
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Spastic paraplegia-optic atrophy-neuropathy syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
Myotilin-related myofibrillar myopathy without spheroid body
Spastic paraplegia-optic atrophy-neuropathy syndrome

MYOT
(UniProt - OMIM)
 TFG
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MYOT
(0.63)
TFG


Citations in the biomedical literature:


Myotilin-related myofibrillar myopathy without spheroid body
MYOT
Spastic paraplegia-optic atrophy-neuropathy syndrome
TFG



Myotilin-related myofibrillar myopathy without spheroid body
Spastic paraplegia-optic atrophy-neuropathy syndrome

Synonym(s):
(no synonyms)

Synonym(s):
- SPOAN
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare eye disease
- 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.