Phenotype #0000204154

Individual ID 00266385
Associated disease TAM1
Phenotype details Lower limb weakness, myalgia, eye movement defects. Muscle biopsy: tubular aggregates, fiber size variability, internal nuclei, fibrosis
Diagnosis/Initial -
Inheritance Isolated (sporadic)
Diagnosis/Definite TAM-1
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johann Böhm
Database submission license No license selected
Created by Johann Böhm
Date created 2019-10-25 12:19:58 +02:00 (CEST)
Date last edited N/A

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