Disease #00230 (AS (Angelman syndrome (AS)), OMIM:105830)

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	Curator: Johan T. den Dunnen

Official abbreviation	AS
Name	Angelman syndrome (AS)
OMIM ID	105830
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	CDKL5, MECP2, UBE3A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2013-10-09 19:24:15 +02:00 (CEST)
Date last edited	N/A