Phenotype #0000228347

Individual ID 00301036
Associated disease APRTD
Phenotype details -
Diagnosis/Initial APRT deficiency
Inheritance Familial, autosomal recessive
Diagnosis/Definite APRTD
Age/Examination -
Age/Diagnosis -
Age/Onset 05y
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 2020-05-05 17:04:06 +02:00 (CEST)
Date last edited 2020-05-05 17:06:49 +02:00 (CEST)

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