Disease #00009 (LYNCH5 (LYNCH SYNDROME 5), OMIM:614350)
Official abbreviation |
LYNCH5 |
Name |
LYNCH SYNDROME 5 |
OMIM ID |
614350 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal dominant |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
MSH6 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
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