FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term cataract 9 multiple types ID (Ontology) DOID:0110266 (Human Disease)
Definition A cataract that has_material_basis_in autosomal recessive or autosomal dominant inheritance of heterozygous or homozygous mutation in the CRYAA gene, which encodes alpha-A-crystallin, on chromosome 21q22.
Also Known As "cataract 9 multiple types with or without microcornea" ; "CTRCT9"
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 Genes
 cataract 9 multiple types      11
 for disease ribbon | cataract 9 multiple types      11
 model of | cataract 9 multiple types      11
Spanning Tree (Parents/Children)
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monogenic disease
 |__cataract_____________________
autosomal genetic disease        |
 |__autosomal dominant disease___|
 |__autosomal recessive disease__|
lens disease                     |
 |__cataract_____________________|
                                 cataract 9 multiple types  11 rec.
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Is a autosomal dominant disease
autosomal recessive disease
cataract
Part of
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Synonyms
  • "autosomal recessive congenital cataract 1" NARROW
    "cataract 9 multiple types with or without microcornea" EXACT
    "CATC1" NARROW OMO:0003012
    "CTRCT9" EXACT OMO:0003012
Secondary IDs
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ICD10CM:Q12.0
MIM:604219