Phenotype #0000252699

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	00334952
Associated disease	Apert
Phenotype details	-
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	Apert Syndrome
Age/Examination	-
Age/Diagnosis	00y11m
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Malak Alghamdi
Database submission license	No license selected
Created by	Malak Alghamdi
Date created	2021-03-02 14:57:54 +01:00 (CET)
Date last edited	2021-03-03 09:17:10 +01:00 (CET)

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