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Metadata
ID	DOID:0070638
Name	mirror movements 4
Definition	A congenital mirror movement disorder that has_material_basis_in heterozygous mutation in the NTN1 gene on chromosome 17p13. https://pmc.ncbi.nlm.nih.gov/articles/PMC5663368/
Xrefs	MIM:618264
SKOS	exactMatch MIM:618264
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