All diseases

OMIM ID
167320
OMIM term:
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA; IBMPFD
Alternative terms:
MUSCULAR DYSTROPHY, LIMB-GIRDLE, WITH PAGET DISEASE OF BONE
PAGETOID AMYOTROPHIC LATERAL SCLEROSIS
PAGETOID NEUROSKELETAL SYNDROME
LOWER MOTOR NEURON DEGENERATION WITH PAGET-LIKE BONE DISEASE
(∗) Location:
9p13.3  
(†) Associated OMIM genes:
VCP  
(‡) Associated MGI genes:
Vcp  

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* quick link - http://q.sanger.ac.uk/akk9l089