Version: 8.0.0
Date: Tue Jan 28 2025
inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3
DOID:0111386
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 3

Definition
An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that has_material_basis_in heterozygous mutation in the HNRNPA1 gene on chromosome 12q13.13.
Synonyms
  • IBMPFD3
  • MSP3
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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      Associated Models

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