Phenotype #0000042983

Individual ID 00056370
Associated disease CNM1
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
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 2013-06-12 15:07:54 +02:00 (CEST)
Date last edited 2013-06-14 10:50:09 +02:00 (CEST)

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