Phenotype #0000309914

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00418577
Associated disease	SGS
Phenotype details	see paper (extensive phenotyping)
Diagnosis/Initial	Shprintzen-Goldberg craniosynostosis syndrome
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	SGS
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2022-09-30 10:17:41 +02:00 (CEST)
Date last edited	N/A

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