Phenotype #0000002251

Individual ID 00003456
Associated disease NPHS2
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Olivier Gribouval
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2013-11-10 21:21:29 +01:00 (CET)
Date last edited N/A

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