Global Variome shared LOVD

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

Phenotype #0000238933 Individual ID 00315181 Associated disease kidney disease Diagnosis/Initial renal hypolasia Diagnosis/Definite - Phenotype details no eye anomalies; renal hypoplasia-unilateral, poor corticomedullary differentiation-unilateral, echogenic cortices; hypotonia; prenatal oligohydramnios, poorly visualized kidneys on ultrasound; 35w-delivery; 1m-end stage renal disease Inheritance Isolated (sporadic) Age/Examination - Age/Diagnosis 5m Age/Onset 1m Phenotype/Onset - Owner name Matthew Bower Database submission license No license selected Created by Matthew Bower Date created 2011-06-23 20:02:56 +02:00 (CEST) Date last edited 2012-01-09 18:09:41 +01:00 (CET)

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