Phenotype #0000351769

Individual ID 00466405
Associated disease NEDHRIT
Diagnosis/Initial Congenital myopathy
Diagnosis/Definite NEDHRIT
Phenotype details Motor delay * Exercise intolerance * Muscular hypotonia * Congenital myopathy
Inheritance Isolated (sporadic)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Owner name Camille Verebi
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Camille Verebi
Date created 2025-08-27 13:38:37 +02:00 (CEST)
Date last edited 2026-02-06 10:21:15 +01:00 (CET)

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