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Summary Literature (0)
DOID:0060193 - amyotrophic lateral sclerosis type 1

Disease Ontology Definition:The most common type of familial ALS that has material basis in mutation in the SOD1 gene on chromosome 21.

Synonyms: ALS1; amyotrophic lateral sclerosis 1

Referenced OMIM:

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : prph, nefh, sod1, dctn1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): amyotrophic lateral sclerosis (is_a)

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