Search Ontology:
Human Disease

inclusion body myopathy with Paget disease of bone and frontotemporal dementia

Term ID
DOID:0050881
Synonyms
  • IBMPFD
  • inclusion body myopathy with Paget's disease of bone and frontotemporal dementia
Definition
A syndrome that is characterized by progressive proximal muscle weakness, steolytic bone lesions consistent with Paget disease, and frontotemporal dementia and has_material_basis_in mutation in the valosin containing protein. (4)
References
Ontology
Human Disease   ( DOID:0050881 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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