Phenotype #0000027270

Individual ID 00033872
Associated disease CTRCT
Phenotype details central nuclear
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 2007-06-21 20:00:00 +02:00 (CEST)
Date last edited 2012-05-18 13:59:33 +02:00 (CEST)

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