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 |
- |
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