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Disease Ontology Browser
amyotrophic lateral sclerosis type 20 (DOID:0060211)
Alliance: disease page
Synonyms: ALS20; amyotrophic lateral sclerosis 20
Alt IDs: OMIM:615426
Definition: An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the HNRNPA1 gene on chromosome 12.


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
11/26/2019
MGI 6.14
The Jackson Laboratory