Disease #05855 (NS10 (Noonan syndrome, type 10 (NS10)), OMIM:616564)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	NS10
Name	Noonan syndrome, type 10 (NS10)
OMIM ID	616564
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LZTR1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-10-16 09:47:45 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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