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Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
3 OMIM references -
3 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Peripheral primitive neuroectodermal tumor
2 associated genes
No signs/symptoms info
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Peripheral primitive neuroectodermal tumor

HNRNPA1
(UniProt - OMIM)
 ERG
(UniProt - OMIM)
HNRNPA2B1
(UniProt - OMIM)
 FLI1
(UniProt - OMIM)
VCP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
HNRNPA2B1
HNRNPA1
(0.78)
(0.68)
ERG
ERG


Citations in the biomedical literature:


Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
HNRNPA1 HNRNPA2B1 VCP
Peripheral primitive neuroectodermal tumor
ERG FLI1



Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Peripheral primitive neuroectodermal tumor

Synonym(s):
- IBMPFD
- Limb-girdle muscular dystrophy with Paget disease of bone
- Pagetoid amyotrophic lateral sclerosis
- Pagetoid neuroskeletal syndrome
Synonym(s):
- PPNET
- Peripheral PNET
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare bone disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal dominant
Epidemiological data:
(no data available)
External references:
3 OMIM references -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.