Global Variome shared LOVD

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

Phenotype #0000306885 Individual ID 00415084 Associated disease CMT2O Phenotype details Sensory axonal neuropathy Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2022-08-08 07:36:34 +02:00 (CEST) Date last edited 2022-08-11 15:54:57 +02:00 (CEST)

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