Phenotype #0000199363

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	00260831
Associated disease	JBTS1
Inheritance	Familial, autosomal recessive
Phenotype details	IMD28; IFNGR2 deficiency; MSMD
Diagnosis/Initial	-
Age/Examination	-
Diagnosis/Definite	-
Age/Diagnosis	-
Age/Onset	-
Phenotype/Onset	-
Protein	-
Owner name	LOVD
Database submission license	No license selected
Created by	Esther van de Vosse
Date created	2017-08-29 15:21:34 +02:00 (CEST)
Date last edited	N/A

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