Search Ontology:
Human Disease

cranioectodermal dysplasia

Term ID
DOID:0050577
Synonyms
  • Levin syndrome
  • Sensenbrenner syndrome
Definition
A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies. (2)
References
Ontology
Human Disease   ( DOID:0050577 )
Relationships
is a type of
has subtype
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Genes Involved
Zebrafish Models