NM_007126.5(VCP):c.*217G>T AND Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001168855.4
Allele description [Variation Report for NM_007126.5(VCP):c.*217G>T]
NM_007126.5(VCP):c.*217G>T
Condition(s)
- Name:
- Inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1
- Synonyms:
- MULTISYSTEM PROTEINOPATHY 1; Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1; Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia 1
- Identifiers:
- MONDO: MONDO:0008178; MedGen: C4551951; OMIM: 167320
Assertion and evidence details
Last Updated: Aug 5, 2023