| General Information | |||
|---|---|---|---|
| Term | lateral sclerosis | ID (Ontology) | DOID:230 (Human Disease) |
| Definition | A motor neuron disease characterized by painless but progressive weakness and stiffness of the muscles of the legs. | ||
| Also Known As | "adult-onset primary lateral sclerosis" ; "primary lateral sclerosis" | ||
| Comment | |||
| Links to External Ontologies | |||
| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
|||
|
No relevant statements available
|
|||
|
||||||
neurodegenerative disease |__motor neuron disease |__lateral sclerosis |
| Spanning Tree View Settings | |||
|---|---|---|---|
| Parents/Children View Depth |
|||
Relationships
|
|||
| Is a | motor neuron disease | ||
| Part of | |||
Synonyms & Secondary IDs
|
|||
| Synonyms | |||
|
|||
| Secondary IDs | |||
|
|
|||
External Crossreferences & Linkouts
|
|||
|
ICD10CM:G12.23 ICD9CM:335.24 MESH:D016472 MIM:611637 NCI:C129933 ORDO:35689 SNOMEDCT_US_2023_03_01:81211007 UMLS_CUI:C0154682 |
|||