Disease #00003

Official abbreviation IBMPFD
Name Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
OMIM ID 167320
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes CHMP2B, VCP
Associated tissues -
Disease features -
Remarks -

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