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Standards Ontologies Notations
amyotrophic lateral sclerosis type 19

Summary
Synonym
  • ALS19
  • amyotrophic lateral sclerosis 19
Definition
An amyotrophic lateral sclerosis that has_material_basis_in mutation in the ERBB4 gene on chromosome 2.
Super Class
amyotrophic lateral sclerosis
Disease Ontology
DOID:0060210
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
2066 ERBB4 erb-b2 receptor tyrosine kinase 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
13869 Erbb4 erb-b2 receptor tyrosine kinase 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
59323 Erbb4 erb-b2 receptor tyrosine kinase 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
37455 Egfr Epidermal growth factor receptor
Displaying 1 entry
Gene ID Gene Symbol Description Source
174462 let-23 Receptor tyrosine-protein kinase let-23;receptor protein-tyrosine kinase
The Human Phenotype Ontology
Displaying entries 1 - 10 of 36 in total
HPO ID HPO Term
HP:0001260 Dysarthria
HP:0002380 Fasciculations
HP:0000713 Agitation
HP:0002094 Dyspnea
HP:0000708 Atypical behavior
HP:0002015 Dysphagia
HP:0002180 Neurodegeneration
HP:0000739 Anxiety
HP:0000217 Xerostomia
HP:0001347 Hyperreflexia
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