Disease #00010 (LYNCH4 (LYNCH SYNDROME 4), OMIM:614337)

Official abbreviation LYNCH4
Name LYNCH SYNDROME 4
OMIM ID 614337
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene PMS2
Associated tissues -
Disease features -
Remarks -
Date created 2016-07-08 14:00:19 +00:00 (UTC)
Date last edited 2023-06-16 09:54:19 +00:00 (UTC)

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