Phenotype #0000233123

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Individual ID	00307323
Associated disease	MPOD
Phenotype details	complete myeloperoxidase deficiencysee paper; ...,
Diagnosis/Initial	complete myeloperoxidase deficiency
Inheritance	Familial, autosomal recessive
Diagnosis/Definite	-
Age/Examination	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	Johan den Dunnen
Database submission license
Created by	Johan den Dunnen
Date created	2020-08-10 17:11:16 +02:00 (CEST)
Date last edited	N/A

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