Phenotype #0000127361

Individual ID 00154625
Associated disease RCM
Phenotype details ventricular septal defect
Diagnosis/Initial cardiomyopathy, restrictive
Inheritance Isolated (sporadic)
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 4y
Phenotype/Onset -
Protein -
Owner name Peikuan Cong
Database submission license No license selected
Created by Peikuan Cong
Date created 2011-08-02 16:13:02 +02:00 (CEST)
Date last edited 2011-10-26 11:12:04 +02:00 (CEST)

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