Term Name: holoprosencephaly 4
Synonyms: HPE4
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the TGIF gene on chromosome 18p11.
Ontology: Human Disease [DOID:0110880]   ( DOID:0110880 )

Relationships
is a type of: autosomal dominant disease holoprosencephaly