Phenotype #0000292010

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00398921
Associated disease	MYOP
Diagnosis/Initial	congenital myopathy
Diagnosis/Definite	-
Phenotype details	newborn hypotonia; proximal weaksness, no distal weakness
Inheritance	Familial, autosomal recessive
Age/Examination	15d
Age/Diagnosis	-
Age/Onset	1d
Phenotype/Onset	newborn hypotonia
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2022-01-14 16:20:15 +01:00 (CET)
Date last edited	N/A

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