Item 1 of 1 (back to results)   Inclusion Body Myopathy 3, Autosomal Dominant C565311               MeSH Unique Identifier: C565311 Scope Notes: Mutation in MYHC2A Click here for more information

Current search: C05. Musculoskeletal Diseases: Musculoskeletal Diseases [MESH:D009140] > Joint Diseases [MESH:D007592] > Contracture [MESH:D003286] > Inclusion Body Myopathy 3, Autosomal Dominant [MESH:C565311] × Select any link to see items in a related category. more general categories    information about this item C05. Musculoskeletal Diseases  C05. Musculoskeletal Diseases  Musculoskeletal Diseases [MESH:D009140] (8705)   Joint Diseases [MESH:D007592] (4657)   Contracture [MESH:D003286] (296)   Inclusion Body Myopathy 3, Autosomal Dominant [MESH:C565311] (1)  Muscular Diseases [MESH:D009135] (4071)   Contracture [MESH:D003286] (303)   Inclusion Body Myopathy 3, Autosomal Dominant [MESH:C565311] (1)  Myositis [MESH:D009220] (2071)   Myositis, Inclusion Body [MESH:D018979] (103)   Inclusion Body Myopathy 3, Autosomal Dominant [MESH:C565311] (1) C10. Nervous System Diseases  C10. Nervous System Diseases  Nervous System Diseases [MESH:D009422] (13325)   Cranial Nerve Diseases [MESH:D003389] (2004)   Ocular Motility Disorders [MESH:D015835] (1697)   Ophthalmoplegia [MESH:D009886] (1468)   Inclusion Body Myopathy 3, Autosomal Dominant [MESH:C565311] (1)  Neurologic Manifestations [MESH:D009461] (8964)   Paralysis [MESH:D010243] (2043)   Ophthalmoplegia [MESH:D009886] (1468)   Inclusion Body Myopathy 3, Autosomal Dominant [MESH:C565311] (1)  Neuromuscular Diseases [MESH:D009468] (7336)   Muscular Diseases [MESH:D009135] (3538)   Myositis [MESH:D009220] (2069)   Myositis, Inclusion Body [MESH:D018979] (103)   Inclusion Body Myopathy 3, Autosomal Dominant [MESH:C565311] (1) C11. Eye Diseases  C11. Eye Diseases  Eye Diseases [MESH:D005128] (6245)   Ocular Motility Disorders [MESH:D015835] (1699)   Ophthalmoplegia [MESH:D009886] (1468)   Inclusion Body Myopathy 3, Autosomal Dominant [MESH:C565311] (1) C23. Pathological Conditions, Signs and Symptoms  C23. Pathological Conditions, Signs and Symptoms  Signs and Symptoms [MESH:D012816] (10659)   Neurologic Manifestations [MESH:D009461] (8702)   Paralysis [MESH:D010243] (2298)   Ophthalmoplegia [MESH:D009886] (1468)   Inclusion Body Myopathy 3, Autosomal Dominant [MESH:C565311] (1)