FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term cataract 18 ID (Ontology) DOID:0110238 (Human Disease)
Definition A cataract that has_material_basis_in homozygous mutation in the FYCO1 gene on chromosome 3p21.3.
Also Known As "autosomal recessive congenital cataract 2" ; "cataract 18 autosomal recessive" ; "CATC2" (for all, see Synonyms field below)
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monogenic disease
 |__cataract_____________________
autosomal genetic disease        |
 |__autosomal recessive disease__|
lens disease                     |
 |__cataract_____________________|
                                 cataract 18
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Is a autosomal recessive disease
cataract
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Synonyms
  • "autosomal recessive congenital cataract 2" EXACT
    "cataract 18 autosomal recessive" EXACT
    "CATC2" EXACT OMO:0003012
    "CTRCT18" EXACT OMO:0003012
Secondary IDs
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ICD10CM:Q12.0
MIM:610019