Phenotype #0000080870

Individual ID 00102730
Associated disease CTRCT
Phenotype details Nuclear
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Zongfu Cao
Database submission license No license selected
Created by Zongfu Cao
Date created 2017-04-02 01:48:59 +02:00 (CEST)
Date last edited 2017-04-16 10:47:49 +02:00 (CEST)

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