Phenotype #0000051405

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	00065077
Associated disease	CCTRCT
Phenotype details	anterior segment mesenchymal dysgenesis
Diagnosis/Initial	-
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Deepti Anand
Database submission license	No license selected
Created by	Johan den Dunnen
Date created	2016-05-26 23:10:42 +02:00 (CEST)
Date last edited	N/A

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