Disease #00513 (HNPCC-1;Lynch (cancer, colorectal, nonpolyposis, hereditary, type 1 (HNPCC-1, Lynch syndrome)), OMIM:120435)
| Official abbreviation |
HNPCC-1;Lynch |
| Name |
cancer, colorectal, nonpolyposis, hereditary, type 1 (HNPCC-1, Lynch syndrome) |
| OMIM ID |
120435 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 7 genes |
EPCAM, GALNT12, MLH1, MLH3, MSH2, MSH6, PMS2 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-08-22 11:31:54 +02:00 (CEST) |
| Date last edited |
N/A |
|
