Disease #00010 (LYNCH4 (LYNCH SYNDROME 4), OMIM:614337)
Official abbreviation |
LYNCH4 |
Name |
LYNCH SYNDROME 4 |
OMIM ID |
614337 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
PMS2 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
|