Phenotype #0000155300

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00207523
Associated disease	NEDHCAS
Diagnosis/Initial	-
Diagnosis/Definite	-
Phenotype details	Global developmental delay; muscular hypotonia; febrile seizures; decreased activity of mitochondrial complex II
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Philippe Campeau
Database submission license
Created by	Philippe Campeau
Date created	2018-11-23 18:21:01 +01:00 (CET)
Date last edited	N/A

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