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Disease Ontology Browser
amyotrophic lateral sclerosis type 2 (DOID:0060194)
Alliance: disease page
Synonyms: ALS2; amyotrophic lateral sclerosis 2; amyotrophic lateral sclerosis 2, juvenile
Alt IDs: OMIM:205100, ICD10CM:G12.2
Definition: An amyotrophic lateral sclerosis that has_material_basis_in mutation in the alsin gene on chromosome 2.

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 6.17
The Jackson Laboratory