Phenotype #0000228316

Individual ID 00301005
Associated disease APRTD
Phenotype details complete APRT deficient
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite APRTD
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-05-04 17:42:59 +02:00 (CEST)
Date last edited N/A

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