Disease #05312 (SGMRT (Singleton-Merten syndrome (SGMRT)))

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SGMRT
Name	Singleton-Merten syndrome (SGMRT)
OMIM ID	-
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 2 genes	DDX58, IFIH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2017-07-28 09:32:18 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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