Phenotype #0000027320

Individual ID 00033922
Associated disease CTRCT
Phenotype details congenital
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 2010-06-14 23:33:39 +02:00 (CEST)
Date last edited 2012-05-18 13:59:33 +02:00 (CEST)

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