Phenotype #0000053375

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Individual ID	00073639
Associated disease	MYOP
Phenotype details	muscular hypotrophy and hypotonia, psychomotor delay, ID, congenital cataract,lactic acidosis, mitochondrial disorders
Diagnosis/Initial	-
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Sophie Nambot
Database submission license	No license selected
Created by	Sophie Nambot
Date created	2016-06-13 11:32:56 +02:00 (CEST)
Date last edited	2016-06-17 11:37:23 +02:00 (CEST)

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