Phenotype #0000166306

Individual ID	00217856
Associated disease	MMEO
Phenotype details	Marked axial weakness; feeding difficulties; 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
Created by	Johan den Dunnen
Date created	2010-09-10 15:52:10 +02:00 (CEST)
Date last edited	2012-03-09 19:08:25 +01:00 (CET)

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