Disease #00524 (Apert (Apert syndrome), OMIM:101200)

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Official abbreviation	Apert
Name	Apert syndrome
OMIM ID	101200
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 21:29:30 +02:00 (CEST)
Date last edited	N/A