amyotrophic lateral sclerosis type 4

Summary
Synonym
  • 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
Definition
An amyotrophic lateral sclerosis with juvenile onset that has_material_basis_in mutation in the SETX gene on chromosome 9.
Super Class
amyotrophic lateral sclerosis
External Links
Disease Ontology
DOID:0060196
Mondo Disease Ontology
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 16 of 16 in total
Gene ID Gene Symbol Description Source
10462 CLEC10A C-type lectin domain containing 10A
10724 OGA O-GlcNAcase
10908 PNPLA6 patatin like phospholipase domain containing 6
23098 SARM1 sterile alpha and TIR motif containing 1
54732 TMED9 transmembrane p24 trafficking protein 9
57103 TIGAR TP53 induced glycolysis regulatory phosphatase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024