WormBase Tree Display for DO_term: DOID:332
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| DOID:332 | Name | amyotrophic lateral sclerosis | |
|---|---|---|---|
| Status | Valid | ||
| Definition | A motor neuron disease that is characterized by muscle spasticity, rapidly progressive weakness due to muscle atrophy, difficulty in speaking, swallowing, and breathing. | ||
| Synonym | Exact | ALS | |
| Lou Gehrig's disease | |||
| motor neuron disease, bulbar | |||
| Parent | Is_a | DOID:231 | |
| Child | Is | DOID:0050752 | |
| DOID:0060193 | |||
| DOID:0060194 | |||
| DOID:0060195 | |||
| DOID:0060196 | |||
| DOID:0060197 | |||
| DOID:0060198 | |||
| DOID:0060199 | |||
| DOID:0060200 | |||
| DOID:0060201 | |||
| DOID:0060202 | |||
| DOID:0060203 | |||
| DOID:0060204 | |||
| DOID:0060205 | |||
| DOID:0060206 | |||
| DOID:0060207 | |||
| DOID:0060209 | |||
| DOID:0060210 | |||
| DOID:0060211 | |||
| DOID:0060212 | |||
| DOID:0060213 | |||
| DOID:0060214 | |||
| DOID:0060355 | |||
| DOID:0080225 | |||
| DOID:0080917 | |||
| DOID:0081378 | |||
| DOID:0081379 | |||
| DOID:0081380 | |||
| DOID:0081381 | |||
| DOID:0081382 | |||
| DOID:0110067 | |||
| DOID:0110068 | |||
| DOID:0110069 | |||
| Disease_model_annotation (60) | |||
| Attribute_of (11) |
