FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term cataract 41 ID (Ontology) DOID:0110241 (Human Disease)
Definition A cataract that has_material_basis_in heterozygous mutation in the WFS1 gene on chromosome 4p16.
Also Known As "congenital nuclear type cataract 41" ; "CTRCT41"
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DO.org
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 Genes
 cataract 41       1
 for disease ribbon | cataract 41       1
 model of | cataract 41       1
Spanning Tree (Parents/Children)
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monogenic disease
 |__cataract____________________
autosomal genetic disease       |
 |__autosomal dominant disease__|
lens disease                    |
 |__cataract____________________|
                                cataract 41  1 rec.
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Is a autosomal dominant disease
cataract
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Synonyms
  • "congenital nuclear type cataract 41" EXACT
    "CTRCT41" EXACT OMO:0003012
Secondary IDs
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ICD10CM:Q12.0
MIM:116400