Search Ontology:
Human Disease
amyotrophic lateral sclerosis type 1
- Term ID
- DOID:0060193
- Synonyms
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- ALS1
- amyotrophic lateral sclerosis 1
- Definition
- An amyotrophic lateral sclerosis that has_material_basis_in mutation in the SOD1 gene on chromosome 21. The most common type of familial ALS. http://en.wikipedia.org/wiki/Amyotrophic_lateral_sclerosis
- References
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- ICD10CM:G12.2
- MIM:105400
- Ontology
- Human Disease ( DOID:0060193 )
- is a type of
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