FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term Leber congenital amaurosis 7 ID (Ontology) DOID:0110333 (Human Disease)
Definition A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13.
Also Known As "LCA7"
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
 Leber congenital amaurosis 7       1      1
 for disease ribbon | Leber congenital amaurosis 7       1       --
 model of | Leber congenital amaurosis 7       1       --
Spanning Tree (Parents/Children)
Only view relationship: 
physical disorder
 |__Leber congenital amaurosis__
retinal disease                 |
 |__Leber congenital amaurosis__|
genetic disease                 |
 |__monogenic disease___________|
                                Leber congenital amaurosis 7  2 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a monogenic disease
Leber congenital amaurosis
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "LCA7" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
ICD10CM:H35.5
MIM:613829