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

σπάνια πάθηση

σύνδρομο

hereditary inclusion body myopathy

Μετωποκροταφική άνοια

GENETIC ASSOCIATION

hnRNPA1

HNRPA2B1

Valosin-containing protein

HEALTH SPECIALTY

νευρολογία