Global Variome shared LOVD

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

Phenotype #0000238902 Individual ID 00315150 Associated disease kidney disease Diagnosis/Initial renal hypolasia Diagnosis/Definite - Phenotype details no eye anomalies; bilateral renal hypoplasia; 8y-end stage renal disease Inheritance Isolated (sporadic) Age/Examination - Age/Diagnosis - Age/Onset 3y Phenotype/Onset - Owner name Matthew Bower Database submission license No license selected Created by Matthew Bower Date created 2011-06-22 20:11:39 +02:00 (CEST) Date last edited N/A

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