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ZNF862 function has not been fully characterized.
Fibromatosis, gingival, 6 is associated with mutations in the ZNF862 gene on chromosome 7.
Genetic testing for ZNF862 is available. Testing is considered confirmatory for diagnosis.
No clinical trials have been registered for fibromatosis, gingival, 6.
3 publications have been identified in PubMed for fibromatosis, gingival, 6. Research spans Review / Meta-Analysis (67%) and Gene Therapy / Novel Therapeutics (33%).
Chen X (2026). [PMID: 41386781](https://pubmed.ncbi.nlm.nih.gov/41386781/). *J Clin Periodontol*. [Gene Therapy / Novel Therapeutics]
Koul R (2025). [PMID: 39872188](https://pubmed.ncbi.nlm.nih.gov/39872188/). *Med J Armed Forces India*. [Review / Meta-Analysis]
Jung YU (2025). [PMID: 41278568](https://pubmed.ncbi.nlm.nih.gov/41278568/). *Arch Plast Surg*. [Review / Meta-Analysis]
Data assembled from 4 of 12 sources · Last updated Sep 18, 2026, 11:35 PM UTC
Online Mendelian Inheritance in Man