FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Duane-radial ray syndrome ID (Ontology) DOID:0060747 (Human Disease)
Definition A syndrome characterized by upper limb anomalies, ocular anomalies, and, in some cases, renal anomalies and that has_material_basis_in heterozygous mutation in the SALL4 gene on chromosome 20q13.
Also Known As "acrorenocular syndrome" ; "DR syndrome" ; "Duane anomaly with radial ray abnormalities and deafness" (for all, see Synonyms field below)
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
 Duane-radial ray syndrome       1
 for disease ribbon | Duane-radial ray syndrome       1
 model of | Duane-radial ray syndrome       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
                                Duane-radial ray syndrome  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "acrorenocular syndrome" EXACT
    "DR syndrome" EXACT
    "Duane anomaly with radial ray abnormalities and deafness" EXACT
    "Okihiro syndrome" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:9182
ICD10CM:Q87.8
MIM:607323
ORDO:93293