Term Name: holoprosencephaly 5
Synonyms: HPE5
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the ZIC2 gene on chromosome 13q32.
Ontology: Human Disease [DOID:0110878]   ( DOID:0110878 )

Relationships
is a type of: autosomal dominant disease holoprosencephaly