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Standards Ontologies Notations
nonsyndromic deafness

Summary
Synonym
  • nonsyndromic hearing loss
  • nonsyndromic hereditary hearing loss
Definition
An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms.
Super Class
auditory system disease
External Links
Disease Ontology
DOID:0050563
Mondo Disease Ontology
MeSH
MGI genotype (from TogoID)
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
4041 LRP5 LDL receptor related protein 5
84920 ALG10 ALG10 alpha-1,2-glucosyltransferase
144245 ALG10B ALG10 alpha-1,2-glucosyltransferase B
Displaying all 2 entries
Gene ID Gene Symbol Description Source
16973 Lrp5 low density lipoprotein receptor-related protein 5
380959 Alg10b ALG10 alpha-1,2-glucosyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
245960 Alg10 ALG10, alpha-1,2-glucosyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
326193 Alg10 ALG10 alpha-1,2-glucosyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
100331575 alg10 ALG10 alpha-1,2-mannosyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
548946 alg10 ALG10, alpha-1,2-glucosyltransferase Xenopus tropicalis (tropical clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
172855 algn-10 Dol-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-Dol alpha-1,2-glucosyltransferase
Displaying 1 entry
Gene ID Gene Symbol Description Source
853142 DIE2 dolichyl-P-Glc:Glc(2)Man(9)GlcNAc(2)-PP-dolichol alpha-1,2- glucosyltransferase
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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