amyotrophic lateral sclerosis type 18

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Summary

Literature (0)

DOID:0060209 - amyotrophic lateral sclerosis type 18

Disease Ontology Definition:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the PFN1 gene on chromosome 17.

Synonyms: ALS18, amyotrophic lateral sclerosis 18

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: pfn1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013891 - amyotrophic lateral sclerosis type 18

MONDO:0013891 - amyotrophic lateral sclerosis type 18

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): amyotrophic lateral sclerosis (is_a)