Phenotype #0000084297

Individual ID 00106493
Associated disease MYOP
Phenotype details myopathy, congenital; dilated cardiomyopathy (severe)
Diagnosis/Initial -
Inheritance Unknown
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Tom Winder
Database submission license No license selected
Created by Tom Winder
Date created 2014-09-24 19:56:35 +02:00 (CEST)
Date last edited 2014-09-28 10:47:59 +02:00 (CEST)

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