Phenotype #0000119378

Individual ID 00146731
Associated disease LGMD-2
Inheritance Isolated (sporadic)
Diagnosis/Initial dystrophy, muscular, limb-girdle, autosomal recessive
Age/Examination -
Diagnosis/Definite LGMD-2I
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Phenotype details -
Protein -
Owner name Lab Müller-Reible