amyotrophic lateral sclerosis type 12

Summary
Synonym
  • ALS12
  • amyotrophic lateral sclerosis 12
Definition
An amyotrophic lateral sclerosis that has_material_basis_in mutation in the OPTN gene on chromosome 10.
Super Class
amyotrophic lateral sclerosis
Disease Ontology
DOID:0060203
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
10133 OPTN optineurin
The Human Phenotype Ontology
Displaying entries 11 - 20 of 36 in total
HPO ID HPO Term
HP:0002145 Frontotemporal dementia
HP:0000716 Depression
HP:0002360 Sleep abnormality
HP:0001257 Spasticity
HP:0000712 Emotional lability
HP:0002017 Nausea and vomiting
HP:0002463 Language impairment
HP:0003487 Babinski sign
HP:0012378 Fatigue
HP:0003324 Generalized muscle weakness
Displaying all 6 entries
Gene ID Gene Symbol Description
5444 PON1 paraoxonase 1
5445 PON2 paraoxonase 2
5446 PON3 paraoxonase 3
55830 GLT8D1 glycosyltransferase 8 domain containing 1
7415 VCP valosin containing protein
9896 FIG4 FIG4 phosphoinositide 5-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: December 9, 2024