Phenotype #0000238171

Individual ID 00313848
Associated disease LGMD
Phenotype details proximal muscle weakness lower extremity, involvement proximal muscles upper limb shoulder girdle; serum CK 1674 U/L; 7y-loss ambulation; no cardiac involvement
Diagnosis/Initial limb-girdle muscular dystrophy
Inheritance Familial, autosomal recessive
Diagnosis/Definite LGMD2D
Age/Examination -
Age/Diagnosis -
Age/Onset 04y
Phenotype/Onset -
Protein -
Owner name Ieke Ginjaar
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2020-10-06 12:24:11 +02:00 (CEST)
Date last edited 2020-10-06 12:33:05 +02:00 (CEST)

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