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Metadata
ID	DOID:0070639
Name	mirror movements 3
Definition	A congenital mirror movement disorder that has_material_basis_in homozygous mutation in the DNAL4 gene on chromosome 22q13. https://pubmed.ncbi.nlm.nih.gov/25098561/
Xrefs	MIM:616059
SKOS	exactMatch MIM:616059
Subsets	DO_rare_slim
Parent Relationships	is_a autosomal recessive disease is_a congenital mirror movement disorder
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance