Disease #00949 (craniosynost. (craniosynostosis, nonspecific))

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Official abbreviation	craniosynost.
Name	craniosynostosis, nonspecific
OMIM ID	-
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FGFR2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A