Disease #05893 (SYNS4 (synostoses, multiple syndrome, type 4 (SYNS4)), OMIM:617898)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SYNS4
Name	synostoses, multiple syndrome, type 4 (SYNS4)
OMIM ID	617898
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GDF6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-01-28 13:52:10 +01:00 (CET)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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