Term Name: cranioectodermal dysplasia 4
Synonyms:
Definition: A cranioectodermal dysplasia that has_material_basis_in compound heterozygous mutation in the WDR19 gene on chromosome 4p14.
Ontology: Human Disease [DOID:0080806]   ( DOID:0080806 )

Relationships
is a type of: cranioectodermal dysplasia