|
DOID:0060194 - amyotrophic lateral sclerosis type 2
Disease Ontology Definition:An amyotrophic lateral sclerosis that has_material_basis_in mutation in the alsin gene on chromosome 2.
Synonyms: ALS2, amyotrophic lateral sclerosis 2, amyotrophic lateral sclerosis 2, juvenile,
Xenbase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MONDO:0008780 - amyotrophic lateral sclerosis type 2, juvenile |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
amyotrophic lateral sclerosis (is_a)