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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: 1
Acute myelomonocytic leukemia
2 associated genes
No signs/symptoms info
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Acute myelomonocytic leukemia

HNRNPA1
(UniProt - OMIM)
 FLT3
(UniProt - OMIM)
HNRNPA2B1
(UniProt - OMIM)
 NPM1
(UniProt - OMIM)
VCP
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
VCP
(0.63)
NPM1


Citations in the biomedical literature:


Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
HNRNPA1 HNRNPA2B1 VCP
Acute myelomonocytic leukemia
FLT3 NPM1



Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Acute myelomonocytic leukemia

Synonym(s):
- IBMPFD
- Limb-girdle muscular dystrophy with Paget disease of bone
- Pagetoid amyotrophic lateral sclerosis
- Pagetoid neuroskeletal syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare bone disease
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Diseases of the nervous system -
Classification (ICD10):
- Neoplasms -
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
1 MeSH reference: D015479
No signs/symptoms info available.