9 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:10595 | Charcot-Marie-Tooth disease | A neuromuscular disease that is characterized by a slowly progressive degeneration of the muscles of the foot, lower leg, hand and forearm. |
DOID:0050539 | Charcot-Marie-Tooth disease type 2 | A Charcot-Marie-Tooth disease characterized by abnormalities in the axon of the peripheral nerve cell. |
40 Relations
Relationship |
Parent Term . Identifier |
Child Term . Identifier |
---|---|---|
is_a | DOID:10595 | DOID:0050539 |
is_a | DOID:574 | DOID:0050539 |
is_a | DOID:870 | DOID:0050539 |
is_a | DOID:440 | DOID:0050539 |
is_a | DOID:4 | DOID:0050539 |
is_a | DOID:863 | DOID:0050539 |
is_a | DOID:7 | DOID:0050539 |
is_a | DOID:17 | DOID:0050539 |
is_a | DOID:0050539 | DOID:0051043 |
is_a | DOID:0050539 | DOID:0110154 |
is_a | DOID:0050539 | DOID:0110155 |
is_a | DOID:0050539 | DOID:0110156 |
is_a | DOID:0050539 | DOID:0110157 |
is_a | DOID:0050539 | DOID:0110158 |
is_a | DOID:0050539 | DOID:0110159 |
is_a | DOID:0050539 | DOID:0110160 |
is_a | DOID:0050539 | DOID:0110161 |
is_a | DOID:0050539 | DOID:0110162 |
is_a | DOID:0050539 | DOID:0110163 |
is_a | DOID:0050539 | DOID:0110164 |
is_a | DOID:0050539 | DOID:0110165 |
is_a | DOID:0050539 | DOID:0110166 |
is_a | DOID:0050539 | DOID:0110167 |
is_a | DOID:0050539 | DOID:0110168 |
is_a | DOID:0050539 | DOID:0110169 |
is_a | DOID:0050539 | DOID:0110170 |
is_a | DOID:0050539 | DOID:0110171 |
is_a | DOID:0050539 | DOID:0110173 |
is_a | DOID:0050539 | DOID:0110174 |
is_a | DOID:0050539 | DOID:0110175 |