Term Name: holoprosencephaly 3
Synonyms: HLP3, HPE3
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the SHH gene on chromosome 7q36.
Ontology: Human Disease [DOID:0110875]   ( DOID:0110875 )

Relationships
is a type of: autosomal dominant disease holoprosencephaly