Disease #00149 (SBS (Sebastian syndrome (SBS)), OMIM:605249)

Global Variome shared LOVD

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

Official abbreviation	SBS
Name	Sebastian syndrome (SBS)
OMIM ID	605249
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MYH9
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-06-12 11:22:31 +02:00 (CEST)
Date last edited	2015-12-08 23:54:35 +01:00 (CET)

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