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Disease Ontology Browser
cranioectodermal dysplasia (DOID:0050577)
Alliance: disease page
Synonyms: Levin syndrome; Sensenbrenner syndrome
Alt IDs: MESH:C562966, OMIM:PS218330
Definition: A syndrome that is characterized by characterized by sagittal craniosynostosis and facial, ectodermal, and skeletal anomalies.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/24/2023
MGI 6.22
The Jackson Laboratory