Disease #00016 (NS1 (NOONAN SYNDROME 1), OMIM:163950)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	NS1
Name	NOONAN SYNDROME 1
OMIM ID	163950
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PTPN11
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-07-08 14:31:36 +00:00 (UTC)
Date last edited	2023-06-16 10:00:08 +00:00 (UTC)