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

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)

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