Phenotype #0000106758

Individual ID 00134009
Associated disease LGMD
Phenotype details -
Diagnosis/Initial dystrophy, muscular, limb-girdle (LGMD)
Inheritance Unknown
Diagnosis/Definite LGMD2C
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 2010-11-23 21:33:13 +01:00 (CET)
Date last edited 2020-10-04 11:07:05 +02:00 (CEST)

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