Phenotype #0000343640

Individual ID 00455043
Associated disease LGMD2
Phenotype details see paper; ..., ambulant; facial weakness; elevated CK level (11x)
Diagnosis/Initial limb-girdle muscular dystrophy
Diagnosis/Definite LGMDR1
Inheritance Familial, autosomal recessive
Age/Examination 45y (45 years)
Age/Onset 30y
Phenotype/Onset -
Age/Diagnosis -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2024-10-01 13:29:04 +02:00 (CEST)
Date last edited N/A

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