# inclusion body myopathy with Paget disease of bone and frontotemporal dementia

> syndrome

**Wikidata**: [Q3508770](https://www.wikidata.org/wiki/Q3508770)  
**Source**: https://4ort.xyz/entity/inclusion-body-myopathy-with-paget-disease-of-bone-and-frontotemporal-dementia


## References

1. Disease Ontology
2. Monarch Disease Ontology release 2018-06-29
3. Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein
4. [ClinGen](https://search.clinicalgenome.org/kb/gene-validity/CGGV:assertion_6ea2bc4d-3b58-4b59-a5bc-9d8a96c452cb-2021-12-23T223510.433Z)
5. [Open Targets Platform](https://platform.opentargets.org/evidence/ENSG00000165280/MONDO_0000507)
6. Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
7. [Identifiers.org](https://registry.identifiers.org/registry/doid)