Disease #00008 (LYNCH2 (LYNCH SYNDROME 2), OMIM:609310)

MVZ für Humangenetik Regensburg

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

Official abbreviation	LYNCH2
Name	LYNCH SYNDROME 2
OMIM ID	609310
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MLH1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-07-08 13:57:28 +00:00 (UTC)
Date last edited	2023-06-16 09:35:37 +00:00 (UTC)