Term Name: holoprosencephaly 2
Synonyms: HPE2
Definition: A holoprosencephaly that has_material_basis_in mutation in the homeobox-containing SIX3 gene on chromosome 2p21.
Ontology: Human Disease [DOID:0110872]   ( DOID:0110872 )

Relationships
is a type of: autosomal dominant disease holoprosencephaly