Phenotype #0000228335

Individual ID 00301024
Associated disease APRTD
Phenotype details -
Diagnosis/Initial APRT deficiency
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 2020-05-05 09:05:55 +02:00 (CEST)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.