Term Name: holoprosencephaly 11
Synonyms: HPE11
Definition: A holoprosencephaly that has_material_basis_in heterozygous mutation in the CDON gene on chromosome 11q24.
Ontology: Human Disease [DOID:0110877]   ( DOID:0110877 )

Relationships
is a type of: autosomal dominant disease holoprosencephaly