Disease #00008 (LYNCH2 (LYNCH SYNDROME 2), OMIM:609310)
Official abbreviation |
LYNCH2 |
Name |
LYNCH SYNDROME 2 |
OMIM ID |
609310 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
MLH1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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