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| Term | Cowden syndrome 4 | ID (Ontology) | DOID:0081000 (Human Disease) |
| Definition | A Cowden syndrome that has_material_basis_in heterozygous germline hypermethylation of the KLLN gene on chromosome 10q23. | ||
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| DO.org | |||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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hamartoma syndrome |__Cowden syndrome |__Cowden syndrome 4 |
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| Is a | Cowden syndrome | ||
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| MIM:615107 | |||