Phenotype #0000203273

Individual ID 00265476
Associated disease LGMD
Phenotype details high CK, difficulty walking, seizures
Diagnosis/Initial LGMD
Inheritance Familial, autosomal recessive
Diagnosis/Definite LGMD2F
Age/Examination 10y (10 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 2019-09-26 11:09:23 +02:00 (CEST)
Date last edited 2020-10-04 11:04:50 +02:00 (CEST)

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