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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](img/icons/info1.png)
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)