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Adult-onset proximal spinal muscular atrophy, autosomal dominant
1 OMIM reference -
1 associated gene
24 connected diseases
No signs/symptoms info
Disease Type of connection
Amyotrophic lateral sclerosis
Cataract - intellectual deficit - hypogonadism
Micro syndrome
Cystic fibrosis
Autosomal dominant spastic ataxia 1
Chuvash erythrocytosis
Von Hippel-Lindau disease
Adult-onset distal myopathy due to VCP mutation
Behavioral variant of frontotemporal dementia
Dedifferentiated liposarcoma
Distal myopathy with posterior leg and anterior hand involvement
Estrogen resistance syndrome
Hereditary combined deficiency of vitamin K-dependent clotting factors
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Muscle filaminopathy
Progressive non-fluent aphasia
Semantic dementia
Spastic paraplegia - Paget disease of bone
Well-differentiated liposarcoma
Encephalopathy due to beta-mercaptolactate-cysteine disulfiduria
Familial isolated dilated cardiomyopathy
Neuralgic amyotrophy
Succinyl-CoA:3-ketoacid CoA transferase deficiency
- Finkel disease

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease

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
External references:
1 OMIM reference -
No MeSH references

Gene symbol UniProt reference OMIM reference
VAPB O95292605704
No signs/symptoms info available.