Term Name: cranioectodermal dysplasia 3
Synonyms:
Definition: A cranioectodermal dysplasia that has_material_basis_in homozygous mutation in the IFT43 gene on chromosome 14q24.
Ontology: Human Disease [DOID:0080805]   (DOID:0080805)

Relationships
is a type of: cranioectodermal dysplasia