Global Variome shared LOVD

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Phenotype #0000292894 Individual ID 00399854 Associated disease craniosynost. Phenotype details see paper; ..., craniosynostosis; no branchio-otic syndrome; affected sutures sgittal; borderline short stature, mild anteverted nares Diagnosis/Initial craniosynostosis Inheritance Familial Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2022-01-23 14:40:45 +01:00 (CET) Date last edited N/A

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