Disease #00057 (YAOS (YAO SYNDROME), OMIM:617321)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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	Curator: Florian Bayersdorfer

Official abbreviation	YAOS
Name	YAO SYNDROME
OMIM ID	617321
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Multifactorial
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 3 genes	INS, NLRP3, NOD2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-02-05 11:42:29 +00:00 (UTC)
Date last edited	2023-06-16 09:49:31 +00:00 (UTC)