Phenotype #0000119663

Individual ID 00146617
Associated disease LGMD
Phenotype details intermediate; lost ambulation 17y; CPK 19x
Diagnosis/Initial dystrophy, muscular, limb-girdle
Inheritance Isolated (sporadic)
Diagnosis/Definite LGMD2I
Age/Examination -
Age/Diagnosis -
Age/Onset 5y
Phenotype/Onset -
Protein IHC: DAG1 absent
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 2007-08-31 17:40:57 +02:00 (CEST)
Date last edited 2020-10-04 11:04:50 +02:00 (CEST)

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