Phenotype #0000201938

Individual ID 00264094
Associated disease LGMD
Phenotype details 20y-tired easily, muscle weakness proximal arms/distal legs, raised serum creatine kinase (3481 IU/L)
Diagnosis/Initial limb-girdle muscular dystrophy
Inheritance Familial, autosomal recessive
Diagnosis/Definite LGMD2B
Age/Examination 46y (46 years)
Age/Diagnosis -
Age/Onset -
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 2019-09-10 21:55:26 +02:00 (CEST)
Date last edited 2020-10-04 11:04:50 +02:00 (CEST)

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