Phenotype #0000343691

Individual ID 00455099
Associated disease LGMD2
Inheritance Familial, autosomal recessive
Diagnosis/Initial limb-girdle muscular dystrophy
Age/Examination 31y (31 years)
Diagnosis/Definite LGMDR1
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Phenotype details see paper; ..., dystrophic pattern; muscle weakness shoulder and pelvic-femoral girdles
Protein normal IHC
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 20:00:32 +02:00 (CEST)
Date last edited N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.