Disease #00009 (LYNCH5 (LYNCH SYNDROME 5), OMIM:614350)

MVZ für Humangenetik Regensburg

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

Official abbreviation	LYNCH5
Name	LYNCH SYNDROME 5
OMIM ID	614350
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MSH6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-07-08 13:59:11 +00:00 (UTC)
Date last edited	2023-06-16 09:40:35 +00:00 (UTC)