Disease #00100 (MRTES (MUIR-TORRE SYNDROME), OMIM:158320)

Official abbreviation MRTES
Name MUIR-TORRE SYNDROME
OMIM ID 158320
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 2 genes MLH1, MSH2
Associated tissues -
Disease features -
Remarks -
Date created 2023-06-16 09:36:57 +00:00 (UTC)
Date last edited N/A

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