Disease #00673 (Scaphocephaly, maxillary retrusion, and mental retardation, OMIM:609579)

MyGenome LOVD - This database is for training purposes only

LOVD v.3.0 Build 30 [ Current LOVD status ]
Log in

Official abbreviation	-
Name	Scaphocephaly, maxillary retrusion, and mental retardation
OMIM ID	609579
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	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	N/A