Global Variome shared LOVD

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

Phenotype #0000129822 Individual ID 00164805 Associated disease NPHP3 Phenotype details congenital hepatic fibrosis end stage renal disease Diagnosis/Initial Nephronophthisis Inheritance Familial, autosomal recessive Diagnosis/Definite Nephronophthisis Age/Examination 20y (20 years) Age/Diagnosis - Age/Onset - Phenotype/Onset 13y Protein - Owner name John Sayer Database submission license Creative Commons Attribution 4.0 International Created by John Sayer Date created 2018-06-13 11:33:11 +02:00 (CEST) Date last edited 2018-06-21 13:11:58 +02:00 (CEST)

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