Term Name: mirror movements 1
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.
Ontology: Human Disease [DOID:0070636]   ( DOID:0070636 )

Relationships
is a type of: autosomal dominant disease congenital mirror movement disorder