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Herb Integrative Database
Traditional Medicine Data Platform
Diseases

Amyotrophic Lateral Sclerosis

amyotrophic lateral sclerosis

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Entity Type
Diseases
Relation Groups
2
Relation Preview
16

Basic Information

Grouped by core information, identifiers, and descriptions.

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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.
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