Global Variome shared LOVD

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Phenotype #0000310114 Individual ID 00418817 Associated disease NPHP1 Phenotype details age at renal failure: 19y; age at end-stage renal failure: ; no retinal dystrophy Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite nephronophthisis Age/Examination 19y (19 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name LOVD Database submission license Creative Commons Attribution 4.0 International Created by Anna Tracewska Date created 2022-10-07 14:01:31 +02:00 (CEST) Date last edited N/A

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