Global Variome shared LOVD

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

Phenotype #0000272788 Individual ID 00377636 Associated disease - Phenotype details liver disease, polydactylyoculomotor apraxia, ptosis 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 Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2021-08-02 11:30:27 +02:00 (CEST) Date last edited N/A

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