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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 (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory