Disease #00231 (BWS (Beckwith-Wiedemann syndrome (BWS)), OMIM:130650)

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Official abbreviation	BWS
Name	Beckwith-Wiedemann syndrome (BWS)
OMIM ID	130650
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 4 genes	CDKN1C, H19, KCNQ1OT1, NSD1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-10-09 19:27:53 +02:00 (CEST)
Date last edited	N/A