Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 1 (IBMPFD1)

Alias:

Inclusion Body Myopathy with Early-Onset Paget Disease and Frontotemporal Dementia

Lower Motor Neuron Degeneration with Paget-Like Bone Disease

Pagetoid Amyotrophic Lateral Sclerosis

Pagetoid Neuroskeletal Syndrome

Ibmpfd1

Myopathy, Inclusion Body, with Early-Onset Paget Disease and Frontotemporal Dementia, Type 1

Inclusion Body Myopathy Without Early-Onset Paget Disease and Frontotemporal Dementia 1

Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia Type 1

Inclusion Body Myopathy with Early-Onset Paget Disease and Frontotemporal Dementia 1

Muscular Dystrophy, Limb-Girdle, with Paget Disease of Bone

Limb-Girdle Muscular Dystrophy with Paget Disease of Bone

Multisystem Proteinopathy 1

Msp1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 1, also known as inclusion body myopathy with early-onset paget disease and frontotemporal dementia, is related to inclusion body myopathy with early-onset paget disease of bone with or without frontotemporal dementia 1 and malaria, and has symptoms including back pain and hip pain. An important gene associated with Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 1 is VCP (Valosin Containing Protein). The drugs Vaccines and Immunologic Factors have been mentioned in the context of this disorder. Affiliated tissues include bone and brain, and related phenotypes are facial palsy and aphasia

Related ID：

MALACARDS：INC029

OMIM：167320

MESH：D010001