Phenotype #0000162022

Individual ID 00213568
Associated disease MYOP
Phenotype details -
Diagnosis/Initial myopathy
Inheritance Unknown
Diagnosis/Definite -
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 2010-10-15 22:03:34 +02:00 (CEST)
Date last edited 2012-10-23 21:23:18 +02:00 (CEST)

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