Phenotype #0000015399

Individual ID 00017035
Associated disease NPHP1
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Marianne Vos (LOVD-team)
Database submission license No license selected
Created by Marianne Vos (LOVD-team)
Date created 2014-06-14 11:57:40 +02:00 (CEST)
Date last edited 2016-06-19 17:40:54 +02:00 (CEST)

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