FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term cataract 46 juvenile-onset ID (Ontology) DOID:0110243 (Human Disease)
Definition A cataract that has_material_basis_in homozygous mutation in the LEMD2 gene on chromosome 6p21.
Also Known As "CTRCT46" ; "juvenilae cataract Hutterite type"
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
 cataract 46 juvenile-onset       1
 for disease ribbon | cataract 46 juvenile-onset       1
 model of | cataract 46 juvenile-onset       1
Spanning Tree (Parents/Children)
Only view relationship: 
monogenic disease
 |__cataract_____________________
autosomal genetic disease        |
 |__autosomal recessive disease__|
lens disease                     |
 |__cataract_____________________|
                                 cataract 46 juvenile-onset  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal recessive disease
cataract
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "CTRCT46" EXACT OMO:0003012
    "juvenilae cataract Hutterite type" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
ICD10CM:Q12.0
MIM:212500