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Disease Ontology Browser
amyotrophic lateral sclerosis type 18 (DOID:0060209)
Alliance: disease page
Synonyms: ALS18; amyotrophic lateral sclerosis 18
Alt IDs: OMIM:614808
Definition: An amyotrophic lateral sclerosis that has_material_basis_in mutation in the PFN1 gene on chromosome 17.

Disease References using Mouse Models (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
12/10/2024
MGI 6.24
The Jackson Laboratory