Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000332968 Individual ID 00443631 Associated disease JBTS Phenotype details molar tooth sign; optic nerve hypoplasia; 4y-no kidney anomalies; elevated liver enzymes Diagnosis/Initial Joubert syndrome Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 4y (4 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Johan den Dunnen Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Created by Johan den Dunnen Date created 2023-11-30 08:54:02 +01:00 (CET) Date last edited N/A

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