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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,
Xenbase Genes
:
setx
| 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)