FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term cone-rod dystrophy 2 ID (Ontology) DOID:0111005 (Human Disease)
Definition A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the CRX gene on chromosome 19q13.
Also Known As "cone-rod retinal dystrophy 2" ; "CORD2" ; "CRD2" (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)
Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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 Human Disease Models
 cone-rod dystrophy 2       1      1
 for disease ribbon | cone-rod dystrophy 2       1       --
 model of | cone-rod dystrophy 2       1       --
Spanning Tree (Parents/Children)
Only view relationship: 
monogenic disease_____
retinal degeneration__|
                      cone-rod dystrophy
                       |__cone-rod dystrophy 2  2 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a cone-rod dystrophy
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "cone-rod retinal dystrophy 2" EXACT
    "CORD2" EXACT OMO:0003012
    "CRD2" EXACT OMO:0003012
    "RCRD2" EXACT OMO:0003012
    "retinal cone-rod dystrophy 2" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:6145
MIM:120970