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Summary Literature (0)
DOID:0060196 - amyotrophic lateral sclerosis type 4

Disease Ontology Definition:An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the SETX gene on chromosome 9.

Synonyms: ALS 4, ALS4, amyotrophic lateral sclerosis 4, amyotrophic lateral sclerosis 4, juvenile, dHMN with upper motor neuron signs, distal hereditary motor neuropathy with pyramidal features, distal hereditary motor neuropathy with upper motor neuron signs

Xenbase Genes : setx

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011223 - amyotrophic lateral sclerosis type 4


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)