Phenotype #0000125738

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00153010
Associated disease	CMS
Phenotype details	global developmental delay, hypotonia, gait problems, weakness
Diagnosis/Initial	syndrome, myasthenic, congenital
Inheritance	Familial, autosomal dominant
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Tom Winder
Database submission license	No license selected
Created by	Tom Winder
Date created	2014-06-03 17:18:46 +02:00 (CEST)
Date last edited	2014-06-06 17:18:28 +02:00 (CEST)

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