FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Axenfeld-Rieger syndrome ID (Ontology) DOID:14686 (Human Disease)
Definition An eye disease characterized by abnormalities of the front part of the eye, the anterior segment.
Also Known As "Anomaly, Rieger's" ; "Axenfeld syndrome" ; "RGS - Rieger syndrome" (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
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship: 
sensory system disease
 |__eye disease_________________
autosomal genetic disease       |
 |__autosomal dominant disease__|
                                Axenfeld-Rieger syndrome  2 rec.
                                 |__Axenfeld-Rieger syndrome type 1 1 rec.
                                 |__Axenfeld-Rieger syndrome type 2
                                 |__Axenfeld-Rieger syndrome type 3 1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
eye disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Anomaly, Rieger's" EXACT
    "Axenfeld syndrome" EXACT
    "Hagedoom syndrome" RELATED
    "RGS - Rieger syndrome" EXACT
    "Rieger's anomaly" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:5701
ICD10CM:Q13.81
MESH:C535679
MIM:PS180500
NCI:C131001
ORDO:782
SNOMEDCT_US_2023_03_01:47507006
UMLS_CUI:C0265341