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Disease Ontology Browser
amyotrophic lateral sclerosis type 1 (DOID:0060193)
Alliance: disease page
Synonyms: ALS1; amyotrophic lateral sclerosis 1
Alt IDs: OMIM:105400, ICD10CM:G12.2
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.

Disease References using Mouse Models (198)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
MGI 6.22
The Jackson Laboratory