14 Parents
| Identifier | Name | Description |
|---|---|---|
| DOID:7 | disease of anatomical entity | A disease that manifests in a defined anatomical structure. |
| DOID:4 | disease | A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism. |
| DOID:863 | nervous system disease | A disease of anatomical entity that is located_in the central nervous system or located_in the peripheral nervous system. |
| DOID:574 | peripheral nervous system disease | A nervous system disease that affects the peripheral nervous system. |
| DOID:17 | musculoskeletal system disease | A disease of anatomical entity that occurs in the muscular and/or skeletal system. |
| DOID:870 | neuropathy | A nervous system disease that is located_in nerves or nerve cells. |
| DOID:440 | neuromuscular disease | A neuropathy that affect the nerves that control the voluntary muscles. |
| DOID:9884 | muscular dystrophy | A myopathy is characterized by progressive skeletal muscle weakness degeneration. |
| DOID:423 | myopathy | A muscular disease in which the muscle fibers do not function resulting in muscular weakness. |
| DOID:66 | muscle tissue disease | A muscular disease located in the muscle tissue. |
| DOID:913 | atrophic muscular disease | A neuromuscular disease that is characterized by an abnormal reduction in the muscle volume and atrophy. |
| DOID:0080000 | muscular disease | A musculoskeletal system disease that affects the muscles. |
| DOID:0050692 | Brody myopathy | A neuromuscular disease is characterized by difficulty relaxing muscles and muscle stiffness following exercise or other strenuous activity and is located in skeletal muscles. |
| DOID:11724 | limb-girdle muscular dystrophy | A muscular dystrophy that is characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles. |
43 Relations
| Relationship |
Parent Term . Identifier |
Child Term . Identifier |
|---|---|---|
| is_a | DOID:11724 | DOID:0080762 |
| is_a | DOID:11724 | DOID:0110273 |
| is_a | DOID:11724 | DOID:0110274 |
| is_a | DOID:11724 | DOID:0110275 |
| is_a | DOID:11724 | DOID:0110276 |
| is_a | DOID:11724 | DOID:0110277 |
| is_a | DOID:11724 | DOID:0110278 |
| is_a | DOID:11724 | DOID:0110279 |
| is_a | DOID:11724 | DOID:0110280 |
| is_a | DOID:11724 | DOID:0110281 |
| is_a | DOID:11724 | DOID:0110282 |
| is_a | DOID:11724 | DOID:0110283 |
| is_a | DOID:11724 | DOID:0110284 |
| is_a | DOID:11724 | DOID:0110285 |
| is_a | DOID:11724 | DOID:0110287 |
| is_a | DOID:11724 | DOID:0110288 |
| is_a | DOID:11724 | DOID:0110289 |
| is_a | DOID:11724 | DOID:0110290 |
| is_a | DOID:11724 | DOID:0110292 |
| is_a | DOID:11724 | DOID:0110293 |
| is_a | DOID:11724 | DOID:0110294 |
| is_a | DOID:11724 | DOID:0110295 |
| is_a | DOID:11724 | DOID:0110296 |
| is_a | DOID:11724 | DOID:0110297 |
| is_a | DOID:11724 | DOID:0110298 |
| is_a | DOID:11724 | DOID:0110299 |
| is_a | DOID:11724 | DOID:0110303 |
| is_a | DOID:11724 | DOID:0110304 |
| is_a | DOID:11724 | DOID:0110305 |
| is_a | DOID:11724 | DOID:0110306 |
