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

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 -

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