Phenotype #0000156029

Individual ID 00035130
Associated disease ?
Diagnosis/Initial LGMD?
Diagnosis/Definite -
Phenotype details suspected limb-gurdle muscular dystrophy, myopathy found in biopsy; family history: sister: LGMD2I (verified genetically), patient: no detection of mutation in the FKRP-gene (2x)
Inheritance Unknown
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Andreas Laner
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2015-04-02 13:01:39 +02:00 (CEST)
Date last edited N/A

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