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, 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,

Echinobase Genes :


OMIM:

MIM:602433 - amyotrophic lateral sclerosis 4, juvenile; als4

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

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