Phenotype #0000272777

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curators: Andreas Laner and Theresa Neuhann

Individual ID	00377625
Associated disease	-
Phenotype details	liver disease, oculomotor apraxia, strabismus
Diagnosis/Initial	Joubert syndrome
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license
Created by	Anna Tracewska
Date created	2021-08-02 11:30:27 +02:00 (CEST)
Date last edited	N/A

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