inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 2

Summary
Synonym
  • IBMPFD2
  • MSP2
  • multisystem proteinopathy 2
Definition
An inclusion body myopathy with Paget disease of bone and frontotemporal dementia that has_material_basis_in heterozygous mutation in HNRPA2B1 on 7p15.2.
Super Class
autosomal dominant disease inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Disease Ontology
DOID:0111384
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3181 HNRNPA2B1 heterogeneous nuclear ribonucleoprotein A2/B1
The Human Phenotype Ontology
Displaying entries 41 - 42 of 42 in total
HPO ID HPO Term
HP:0012444 Brain atrophy
HP:0012548 Fatty replacement of skeletal muscle
Displaying 1 entry
Gene ID Gene Symbol Description
7415 VCP valosin containing protein

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024