Search Ontology:
Human Disease

mirror movements 1

Term ID
DOID:0070636
Synonyms
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. (3)
References
Ontology
Human Disease   ( DOID:0070636 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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