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Metadata
ID	DOID:0070637
Name	mirror movements 2
Definition	A congenital mirror movement disorder that has_material_basis_in heterozygous mutation in the RAD51 gene on chromosome 15q15. https://pmc.ncbi.nlm.nih.gov/articles/PMC5099496/
Xrefs	MIM:614508
SKOS	exactMatch MIM:614508
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