FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term cataract 16 multiple types ID (Ontology) DOID:0110250 (Human Disease)
Definition A cataract that has_material_basis_in heterozygous or homozygous mutation in the CRYAB gene on chromosome 11q.
Also Known As "CTRCT16"
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 Genes
 cataract 16 multiple types       2
 for disease ribbon | cataract 16 multiple types       2
 model of | cataract 16 multiple types       2
Spanning Tree (Parents/Children)
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monogenic disease
 |__cataract_____________________
autosomal genetic disease        |
 |__autosomal dominant disease___|
 |__autosomal recessive disease__|
lens disease                     |
 |__cataract_____________________|
                                 cataract 16 multiple types  2 rec.
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Is a autosomal dominant disease
autosomal recessive disease
cataract
Part of
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Synonyms
  • "CTPP2" NARROW OMO:0003012
    "CTRCT16" EXACT OMO:0003012
    "posterior polar cataract 2" NARROW
Secondary IDs
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ICD10CM:Q12.0
MIM:613763