BabelNet

bn:04726731n

Noun Concept

No term available

Syndrome that is characterized by progressive proximal muscle weakness, steolytic bone lesions consistent with Paget disease, and frontotemporal dementia and has physical basis in mutation in the valosin containing protein (VCP) Wikidata

Relations

Sources

IS A

zeldzame ziekte

syndroom

hereditary inclusion body myopathy

frontotemporale dementie

GENETIC ASSOCIATION

HEALTH SPECIALTY