Disease #07064 (NS14 (Noonan syndrome, type 14), OMIM:619745)

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	NS14
Name	Noonan syndrome, type 14
OMIM ID	619745
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SPRED2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-01-25 09:32:16 +01:00 (CET)
Date last edited	N/A

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