Term Name: congenital heart defects, dysmorphic facial features, and intellectual developmental disorder
Synonyms: CDK13-Related CHDFIDD, CDK13-Related Disorder, CHDFIDD
Definition: A syndrome characterized by congenital heart defects, dysmorphic facial features, and impaired intellectual developmental that has_material_basis_in heterozygous mutation in the CDK13 gene on chromosome 7p14.1.
Ontology: Human Disease [DOID:0112247]   ( DOID:0112247 )

Relationships
is a type of: autosomal dominant disease syndrome