Disease #00525 (Crouzon (Crouzon syndrome), OMIM:123500)

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Official abbreviation	Crouzon
Name	Crouzon syndrome
OMIM ID	123500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FGFR2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-16 21:35:03 +02:00 (CEST)
Date last edited	N/A