Disease #00383 (NS1 (Noonan syndrome 1 (NS1)), OMIM:163950)

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	Curator: Johan T. den Dunnen

Official abbreviation	NS1
Name	Noonan syndrome 1 (NS1)
OMIM ID	163950
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PTPN11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-05-14 14:26:30 +02:00 (CEST)
Date last edited	N/A