FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term X-linked cone-rod dystrophy 3 ID (Ontology) DOID:0111007 (Human Disease)
Definition A cone-rod dystrophy that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.
Also Known As "CORDX3"
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DO.org
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 Genes
 X-linked cone-rod dystrophy 3       1
 for disease ribbon | X-linked cone-rod dystrophy 3       1
 model of | X-linked cone-rod dystrophy 3       1
Spanning Tree (Parents/Children)
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monogenic disease
 |__cone-rod dystrophy__________
X-linked monogenic disease      |
 |__X-linked recessive disease__|
retinal degeneration            |
 |__cone-rod dystrophy__________|
                                X-linked cone-rod dystrophy 3  1 rec.
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Is a cone-rod dystrophy
X-linked recessive disease
Part of
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Synonyms
  • "CORDX3" EXACT OMO:0003012
Secondary IDs
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MIM:300476