Phenotype #0000162000

Individual ID 00213546
Associated disease CMYO4A;CFTD
Phenotype details see paper; ...
Diagnosis/Initial myopathy, congenital, with fiber-type disproportion
Inheritance Isolated (sporadic)
Diagnosis/Definite CFTD
Age/Examination -
Age/Diagnosis -
Age/Onset <0d
Phenotype/Onset reduced fetal movement
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 2015-12-14 00:26:52 +01:00 (CET)
Date last edited N/A

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