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Metadata
ID	DOID:0070636
Name	mirror movements 1
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. https://pubmed.ncbi.nlm.nih.gov/31697046/, https://pubmed.ncbi.nlm.nih.gov/20431009/, https://pmc.ncbi.nlm.nih.gov/articles/PMC5894478/
Xrefs	MIM:157600
SKOS	exactMatch MIM:157600
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal dominant disease is_a congenital mirror movement disorder
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance