Phenotype #0000357053

Individual ID 00472244
Associated disease ?
Diagnosis/Initial LGMD
Diagnosis/Definite Multiple mitochondrial dysfunctions syndrome 10
Phenotype details 0006785: Limb-girdle muscular dystrophy, 011807: Type 1 muscle fibre atrophy, 0002515: Waddling gait, 0410011: Abnormality of masticatory muscle
Inheritance Unknown
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 2026-01-19 17:28:07 +01:00 (CET)
Date last edited 2026-02-06 10:21:15 +01:00 (CET)

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