Disease #03939 (IBMPFD-2 (myopathy, inclusion body, with early-onset Paget disease with or without frontotemporal dementia, type 2 (IBMPFD-2)), OMIM:615422)

Official abbreviation IBMPFD-2
Name myopathy, inclusion body, with early-onset Paget disease with or without frontotemporal dementia, type 2 (IBMPFD-2)
OMIM ID 615422
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene HNRNPA2B1
Associated tissues -
Disease features -
Remarks -