FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term cataract 40 ID (Ontology) DOID:0110272 (Human Disease)
Definition A cataract that has_material_basis_in mutation in the NHS gene on chromosome Xp22.
Also Known As "cataract 40 with or without microcornea" ; "cataract 40 X-linked" ; "CTRCT40"
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 40       1
 for disease ribbon | cataract 40       1
 model of | cataract 40       1
Spanning Tree (Parents/Children)
Only view relationship:
monogenic disease
 |__X-linked monogenic disease__
 |__cataract____________________|
lens disease                    |
 |__cataract____________________|
                                cataract 40  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a X-linked monogenic disease
cataract
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "cataract 40 with or without microcornea" EXACT
    "cataract 40 X-linked" EXACT
    "CTRCT40" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
ICD10CM:Q12.0
MIM:302200