Global Variome shared LOVD

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

Phenotype #0000321077 Individual ID 00430268 Associated disease CMT2T Phenotype details - Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 66 Age/Diagnosis - Age/Onset 50y? Phenotype/Onset walking difficulties Protein - Owner name Marco Savarese Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International Created by Marco Savarese Date created 2023-01-16 16:30:30 +01:00 (CET) Date last edited 2023-01-17 12:00:41 +01:00 (CET)

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