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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.12
The Jackson Laboratory