Term Name: craniosynostosis 3
Synonyms: CRS3
Definition: A craniosynostosis that has_material_basis_in heterozygous mutation in the TCF12 gene on chromosome 15q21.
Ontology: Human Disease [DOID:0061011]   ( DOID:0061011 )

Relationships
is a type of: autosomal dominant disease craniosynostosis