Phenotype #0000162023

Individual ID 00213569
Associated disease CMYO4A;CFTD
Phenotype details hypotonia, axial weakness, FTT, muscle biopsy shows CFTD
Diagnosis/Initial fiber-type disproportion, congenital
Inheritance Unknown
Diagnosis/Definite CFTD
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Tom Winder
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2011-09-02 22:06:01 +02:00 (CEST)
Date last edited 2013-02-01 19:44:13 +01:00 (CET)

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