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Metadata
ID	DOID:0070295
Name	primary autosomal dominant microcephaly 18
Definition	A primary microcephaly that has_material_basis_in heterozygous mutation in the WDFY3 gene on chromosome 4q21. https://www.ncbi.nlm.nih.gov/pubmed/27008544
Xrefs	OMIM:617520
Synonyms	MCPH18 [EXACT]
Parent Relationships	is_a primary microcephaly is_a autosomal dominant disease