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DO Term : cranioectodermal dysplasia [DOID:0050577] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies.
  • synonyms:
  • Sensenbrenner syndrome,
  • MESH:C562966,
  • OMIM:PS218330,
  • PS218330,
  • Levin syndrome
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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