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Disease Ontology Browser
amyotrophic lateral sclerosis type 4 (DOID:0060196)
Alliance: disease page
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
Alt IDs: OMIM:602433, ICD10CM:G12.2, ORDO:357043
Definition: An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the SETX gene on chromosome 9.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory