Global Variome shared LOVD

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

Phenotype #0000129177 Individual ID 00164068 Associated disease NPHP3 Phenotype details congenital hepatic fibrosis end stage renal disease Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name John Sayer Database submission license Creative Commons Attribution 4.0 International Created by John Sayer Date created 2018-05-09 16:21:26 +02:00 (CEST) Date last edited 2018-05-10 11:33:58 +02:00 (CEST)

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