FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term mirror movements 3 ID (Ontology) DOID:0070639 (Human Disease)
Definition A congenital mirror movement disorder that has_material_basis_in homozygous mutation in the DNAL4 gene on chromosome 22q13.
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 Genes
 mirror movements 3       1
 for disease ribbon | mirror movements 3       1
 model of | mirror movements 3       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal recessive disease__________
physical disorder                        |
 |__congenital mirror movement disorder__|
movement disease                         |
 |__congenital mirror movement disorder__|
                                         mirror movements 3  1 rec.
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Is a autosomal recessive disease
congenital mirror movement disorder
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MIM:616059