Search Ontology:
Human Disease
familial adenomatous polyposis 3
- Term ID
- DOID:0080411
- Synonyms
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- Definition
- A familial adenomatous polyposis that has_material_basis_in homozygous or compound heterozygous mutation in the NTHL1 gene on chromosome 16p13. https://www.ncbi.nlm.nih.gov/pubmed/25938944
- References
- Ontology
- Human Disease ( DOID:0080411 )
- is a type of
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