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Metadata
ID	DOID:0110878
Name	holoprosencephaly 5
Definition	A holoprosencephaly that has_material_basis_in heterozygous mutation in the ZIC2 gene on chromosome 13q32. https://www.ncbi.nlm.nih.gov/pubmed/9771712
Xrefs	MESH:C566464 OMIM:609637
Synonyms	HPE5 [EXACT]
Parent Relationships	is_a holoprosencephaly is_a autosomal dominant disease