Usher syndrome type 1D

Summary
Synonym
  • USH1D
  • Usher syndrome type ID
Definition
An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22.
Super Class
Usher syndrome type 1 digenic disease
Disease Ontology
DOID:0110831
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
64072 CDH23 cadherin related 23
65217 PCDH15 protocadherin related 15
Displaying all 2 entries
Gene ID Gene Symbol Description Source
11994 Pcdh15 protocadherin 15
22295 Cdh23 cadherin related 23 (otocadherin)
Displaying 1 entry
Gene ID Gene Symbol Description Source
114102 Cdh23 cadherin-related 23
Displaying all 2 entries
Gene ID Gene Symbol Description Source
41441 Cad87A Cadherin 87A
43528 Cad99C Cadherin 99C

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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