Search Ontology:
Human Disease
Cowden syndrome 7
- Term ID
- DOID:0081003
- Synonyms
-
- Definition
- A Cowden syndrome that has_material_basis_in heterozygous mutation in the SEC23B gene on chromosome 20p11. https://pubmed.ncbi.nlm.nih.gov/26522472/
- References
- Ontology
- Human Disease ( DOID:0081003 )
- is a type of
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