FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term cataract 14 multiple types ID (Ontology) DOID:0110253 (Human Disease)
Definition A cataract that has_material_basis_in heterozygous mutation in the gene encoding gap junction protein alpha-3 (GJA3) on chromosome 13q12.
Also Known As "CTRCT14"
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DO.org
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monogenic disease
 |__cataract____________________
autosomal genetic disease       |
 |__autosomal dominant disease__|
lens disease                    |
 |__cataract____________________|
                                cataract 14 multiple types
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Is a autosomal dominant disease
cataract
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Synonyms
  • "CAE3" NARROW OMO:0003012
    "CTRCT14" EXACT OMO:0003012
    "CZP3" NARROW OMO:0003012
    "zonular pulverulent cataract 3" NARROW
Secondary IDs
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ICD10CM:Q12.0
MIM:601885