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

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)

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