Disease #00005 (LYNCH1 (LYNCH SYNDROME 1), OMIM:120435)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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	Curators: Admin and Florian Bayersdorfer

Official abbreviation	LYNCH1
Name	LYNCH SYNDROME 1
OMIM ID	120435
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	MSH2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2016-07-05 15:24:13 +00:00 (UTC)
Date last edited	2023-06-16 09:37:39 +00:00 (UTC)