Phenotype #0000166303

Individual ID 00217853
Associated disease MMEO
Phenotype details Marked axial weakness; feeding difficulties; respiratory muscle weakness; walk (18-24m)
Diagnosis/Initial minicore myopathy
Inheritance Isolated (sporadic)
Diagnosis/Definite MMD
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset muscle weakness; hypotonia; feeding problems; delayed motor milestones
Protein -
Owner name Jorge Oliveira
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-09-10 15:52:10 +02:00 (CEST)
Date last edited 2012-03-09 18:27:00 +01:00 (CET)

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