FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term cranioectodermal dysplasia ID (Ontology) DOID:0050577 (Human Disease)
Definition A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies.
Also Known As "Levin syndrome" ; "Sensenbrenner syndrome"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal recessive disease__
disease                          |
 |__syndrome_____________________|
                                 cranioectodermal dysplasia  4 rec.
                                  |__cranioectodermal dysplasia 1 1 rec.
                                  |__cranioectodermal dysplasia 2 1 rec.
                                  |__cranioectodermal dysplasia 3 1 rec.
                                  |__cranioectodermal dysplasia 4 1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal recessive disease
syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Levin syndrome" EXACT
    "Sensenbrenner syndrome" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
MESH:C562966
MIM:PS218330