Phenotype #0000272903

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	00377757
Associated disease	-
Phenotype details	Leber congenital amaurosis,cerebellar vermis hypoplasia
Diagnosis/Initial	Joubert syndrome
Inheritance	Familial
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Julia Lopez
Date created	2021-08-02 20:37:33 +02:00 (CEST)
Date last edited	N/A

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