Phenotype #0000058631

Individual ID 00078872
Associated disease LGMDR12;LGMD2L
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 2013-06-28 23:10:26 +02:00 (CEST)
Date last edited 2013-06-29 20:56:42 +02:00 (CEST)

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