Phenotype #0000158835

Individual ID 00210269
Associated disease RCM
Phenotype details carrier mother MYL2:G57E and MYL3:E143K
Diagnosis/Initial restrictive cardiomyopathy
Inheritance Familial, autosomal recessive
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 2012-03-18 21:48:19 +01:00 (CET)
Date last edited 2012-03-26 16:00:39 +02:00 (CEST)

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