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