Version: 8.0.0
Date: Tue Jan 28 2025
All
All
Gene
Gene Ontology
Disease
Allele/Variant
Model
HTP Dataset Index
Home
Data and Tools
Downloads
API
AllianceMine
JBrowse 2
Submit Data
Textpresso
Tools and Prototypes
COVID-19 Information
Members
FlyBase
Mouse Genome Database
Rat Genome Database
Saccharomyces Genome Database
WormBase
Xenbase
Zebrafish Information Network
Gene Ontology Consortium
News
News and Events
Release Notes
Event Calendar
About
About Us
Funding
Publications
Organization and Governance
Privacy, Warranty, Licensing, and Data Preservation Commitment
Working Groups
Help
FAQ / Known Issues
Glossary
Tutorials
User Documentation
Community
Alliance User Community
Mastodon
Bluesky
Contact Us
Cite Us
Usher syndrome type 1E
DOID:0110833
Summary
Associated Genes
Associated Alleles
Associated Models
Disease
Usher syndrome type 1E
Definition
An Usher syndrome type 1 that has_material_basis_in variation in the chromosome region 21q21.
[1]
Synonyms
USH1E
Usher syndrome type IE
Cross References
ICD10CM:H35.5
MIM:602097
Parent Terms
Usher syndrome type 1
Child Terms
None
Sources of Associations
RGD
MGI
ZFIN
FB
WB
SGD
Associated Genes
No data available
Associated Alleles
No data available
Associated Models
No data available
You need to enable JavaScript to run this app.