Phenotype #0000105568

Individual ID 00132805
Associated disease LQT
Phenotype details see paper, ...
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
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 2017-11-09 17:57:58 +01:00 (CET)
Date last edited 2017-11-09 18:08:27 +01:00 (CET)

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