FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Usher syndrome type 1D ID (Ontology) DOID:0110831 (Human Disease)
Definition An Usher syndrome type 1 that has_material_basis_in homozygous or compound heterozygous mutation in the CDH23 gene on chromosome 10q22.
Also Known As "USH1D" ; "Usher syndrome type ID"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 Usher syndrome type 1D       2
 for disease ribbon | Usher syndrome type 1D       2
 model of | Usher syndrome type 1D       2
Spanning Tree (Parents/Children)
Only view relationship: 
Usher syndrome
 |__Usher syndrome type 1__
polygenic disease          |
 |__digenic disease________|
                           Usher syndrome type 1D  2 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a digenic disease
Usher syndrome type 1
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "USH1D" EXACT OMO:0003012
    "Usher syndrome type ID" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
ICD10CM:H35.5
MIM:601067