Phenotype #0000357020

Individual ID 00472211
Associated disease ?
Diagnosis/Initial Congenital myopathy
Diagnosis/Definite -
Phenotype details Skeletal myopathy, Congenital onset, Central core regions in muscle fibers, Lipoma
Inheritance Isolated (sporadic)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Tumor/MSI -
Diagnosis/Criteria -
Owner name Camille Verebi
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Camille Verebi
Date created 2026-01-16 12:28:23 +01:00 (CET)
Date last edited 2026-02-06 10:21:15 +01:00 (CET)

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