Term Name: cranioectodermal dysplasia
Synonyms: Levin syndrome, Sensenbrenner syndrome
Definition: A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies.
Ontology: Human Disease [DOID:0050577]   ( DOID:0050577 )

Relationships
is a type of: autosomal recessive disease syndrome
has subtype: cranioectodermal dysplasia 1 cranioectodermal dysplasia 2 cranioectodermal dysplasia 3 cranioectodermal dysplasia 4