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 21 ID (Ontology) DOID:0081447 (Human Disease)
Definition A cone-rod dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DRAM2 gene on chromosome 1p13.
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 Genes
 cone-rod dystrophy 21       1
 for disease ribbon | cone-rod dystrophy 21       1
 model of | cone-rod dystrophy 21       1
Spanning Tree (Parents/Children)
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monogenic disease
 |__cone-rod dystrophy___________
autosomal genetic disease        |
 |__autosomal recessive disease__|
retinal degeneration             |
 |__cone-rod dystrophy___________|
                                 cone-rod dystrophy 21  1 rec.
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Is a cone-rod dystrophy
autosomal recessive disease
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MIM:616502