FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term cone-rod dystrophy 12 ID (Ontology) DOID:0111019 (Human Disease)
Definition A cone-rod dystrophy that has_material_basis_in homozygous or heterozygous mutation in the PROM1 gene on chromosome 4p15.
Also Known As "CORD12"
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DO.org
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Data Class Field Records
Human Disease Models (FBhh)  DOID       1
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Relevant FlyBase reports
 Genes Human Disease Models
 cone-rod dystrophy 12       2      1
 for disease ribbon | cone-rod dystrophy 12       2       --
 model of | cone-rod dystrophy 12       2       --
Spanning Tree (Parents/Children)
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monogenic disease_____
retinal degeneration__|
                      cone-rod dystrophy
                       |__cone-rod dystrophy 12  3 rec.
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Is a cone-rod dystrophy
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Synonyms
  • "CORD12" EXACT OMO:0003012
Secondary IDs
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MESH:C567206
MIM:612657