Phenotype #0000232135

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00306289
Associated disease	leukoencephalopathy
Diagnosis/Initial	leukoencephalopathy
Diagnosis/Definite	LCC
Phenotype details	developmental delay and monoparesis; mild hemiplegia
Inheritance	Familial, autosomal recessive
Age/Examination	5y (5 years)
Age/Diagnosis	-
Age/Onset	18m
Phenotype/Onset	developmental delay and monoparesis
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2020-07-13 19:04:44 +02:00 (CEST)
Date last edited	N/A

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