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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Adult-onset proximal spinal muscular atrophy, autosomal dominant
Muscle filaminopathy

VAPB FLNC


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
VAPB
(0.63)
FLNC



Citations in the biomedical literature:


Adult-onset proximal spinal muscular atrophy, autosomal dominant
VAPB
Muscle filaminopathy
FLNC



Adult-onset proximal spinal muscular atrophy, autosomal dominant
Muscle filaminopathy

Synonym(s):
- Finkel disease

Synonym(s):
(no synonyms)

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:
Class of prevalence: 1-9 / 1 000 000
Average age onset: adulthood
Average age of death: -
Type of inheritance: autosomal dominant
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.