FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term mirror movements 1 ID (Ontology) DOID:0070636 (Human Disease)
Definition A congenital mirror movement disorder characterized by mirror movements and/or agenesis of the corpus callosum that has_material_basis_in heterozygous mutation in the DCC gene on chromosome 18q21, with incomplete penetrance.
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Human Disease Models (FBhh)  DOID       1
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 Genes Human Disease Models
 mirror movements 1       1      1
 for disease ribbon | mirror movements 1       1       --
 model of | mirror movements 1       1       --
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease___________
physical disorder                        |
 |__congenital mirror movement disorder__|
movement disease                         |
 |__congenital mirror movement disorder__|
                                         mirror movements 1  2 rec.
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Is a autosomal dominant disease
congenital mirror movement disorder
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MIM:157600