01
FIG4
No data
- Entity Type
- Diseases
- Relation Groups
- 4
- Relation Preview
- 32
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Amyotrophic Lateral Sclerosis
- Standard Disease Name
- amyotrophic lateral sclerosis
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- No data
- OMIM ID
- No data
- UMLS ID
- C0346068
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_02D:A rare congenital but non-hereditary disorder characterized by angiomas or arteriovenous malformations of the spinal cord. Clinical signs include sudden onset of radicular pain localizable to a dermatome with overlying cutaneous vascular lesions. Untreated, the clinical course follows a progression of sensory loss, weakness to paralysis and incontinence. However, clinical prognosis improves with endovascular embolization and/or surgical excision of the spinal lesion.
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.