Phenotype #0000209248

Individual ID 00274303
Associated disease LGMD
Phenotype details markedly elevated CK level; muscle histology dystrophic; non-ambulatory
Diagnosis/Initial LGMD
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset 14y
Phenotype/Onset -
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 2019-12-28 16:38:54 +01:00 (CET)
Date last edited 2019-12-28 17:11:34 +01:00 (CET)

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