Search Ontology:
Human Disease
Cowden syndrome 4
- Term ID
- DOID:0081000
- Synonyms
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- Definition
- A Cowden syndrome that has_material_basis_in heterozygous germline hypermethylation of the KLLN gene on chromosome 10q23. https://pubmed.ncbi.nlm.nih.gov/21177507/
- References
- Ontology
- Human Disease ( DOID:0081000 )
- is a type of
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