Disease #00005 (HNPCC (Lynch syndrome), OMIM:609309)
Official abbreviation |
HNPCC |
Name |
Lynch syndrome |
OMIM ID |
609309 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
7 |
Phenotype entries for this disease |
1 |
Associated with 3 genes |
MSH2, MSX1, PMS2 |
Associated tissues |
colon |
Disease features |
- |
Remarks |
- |
Individuals
|
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