Phenotype #0000237058

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00311803
Associated disease	mitochondrial
Diagnosis/Initial	-
Diagnosis/Definite	Mitochondrial disorder
Phenotype details	neonatal hypertrophic cardiomyopathy encephalopathy severe lactic acidosis Isolated complex IV deficiency
Inheritance	Familial, autosomal recessive
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Owner name	Liesbeth T. Wintjes
Database submission license	No license selected
Created by	Liesbeth T. Wintjes
Date created	2020-09-28 13:45:12 +02:00 (CEST)
Date last edited	2020-09-29 10:46:37 +02:00 (CEST)

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