Disease #05691 (CRS6 (craniosynostosis, type 6 (CRS6)), OMIM:616602)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CRS6
Name	craniosynostosis, type 6 (CRS6)
OMIM ID	616602
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ZIC1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-02-08 13:52:53 +01:00 (CET)
Date last edited	N/A

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