Disease #05690 (CRS7 (craniosynostosis, susceptibility to, type 7 (CRS7)), OMIM:617439)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	CRS7
Name	craniosynostosis, susceptibility to, type 7 (CRS7)
OMIM ID	617439
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SMAD6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-02-08 13:48:44 +01:00 (CET)
Date last edited	N/A

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