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Metadata
ID	DOID:0110875
Name	holoprosencephaly 3
Definition	A holoprosencephaly that has_material_basis_in heterozygous mutation in the SHH gene on chromosome 7q36. https://www.ncbi.nlm.nih.gov/pubmed/8896572
Xrefs	MESH:C564181 MIM:142945
Synonyms	HLP3 [EXACT] HPE3 [EXACT]
Parent Relationships	is_a holoprosencephaly is_a autosomal dominant disease