diff --git a/CHANGELOG.md b/CHANGELOG.md
index 3418f49f7..f95517c4b 100644
--- a/CHANGELOG.md
+++ b/CHANGELOG.md
@@ -20,6 +20,7 @@ Special thanks to the following for their contributions to the release:
 - [PR #1614](https://github.com/nf-core/rnaseq/pull/1614) - Template update for nf-core/tools v3.4.1
 - [PR #1618](https://github.com/nf-core/rnaseq/pull/1618) - Fix CI: Ensure confirm-pass job runs for markdown-only PRs
 - [PR #1617](https://github.com/nf-core/rnaseq/pull/1617) - Update bbmap/bbsplit module
+- [PR #1625](https://github.com/nf-core/rnaseq/pull/1625) - Add documentation warning about Qualimap read counting bug ([#1273](https://github.com/nf-core/rnaseq/issues/1273))
 - [PR #1622](https://github.com/nf-core/rnaseq/pull/1622) - Update tximeta/tximport module to fix sample name mangling
 - [PR #1620](https://github.com/nf-core/rnaseq/pull/1620) - Fix bigwig strand labeling for reverse-stranded libraries ([#1591](https://github.com/nf-core/rnaseq/issues/1591))
 - [PR #1621](https://github.com/nf-core/rnaseq/pull/1621) - Optimize qualimap performance with multi-threaded name sorting
diff --git a/docs/output.md b/docs/output.md
index b47593a05..77b921fb4 100644
--- a/docs/output.md
+++ b/docs/output.md
@@ -614,6 +614,18 @@ RSeQC documentation: [tin.py](http://rseqc.sourceforge.net/#tin-py)
 
 The [Qualimap RNA-seq QC module](http://qualimap.bioinfo.cipf.es/doc_html/analysis.html#rna-seq-qc) is used within this pipeline to assess the overall mapping and coverage relative to gene features.
 
+:::warning
+**Known limitation**: Qualimap has a known bug ([#1273](https://github.com/nf-core/rnaseq/issues/1273), [Qualimap issue #81](https://bitbucket.org/kokonech/qualimap/issues/81)) where it may report more reads assigned to genomic features (exons, introns, intergenic regions) than the total number of reads in the BAM file. This can lead to inflated read counts and incorrect genomic origin statistics.
+
+If accurate read distribution metrics are critical for your analysis, we recommend:
+
+- Cross-referencing Qualimap results with RSeQC output (particularly `read_distribution.txt`)
+- Using `--skip_qualimap` to disable Qualimap and rely on RSeQC for genomic feature distribution
+- Validating suspicious results with alternative tools or custom scripts
+
+This is an upstream tool issue that cannot be fixed at the pipeline level.
+:::
+
 ![MultiQC - Qualimap gene coverage plot](images/mqc_qualimap_coverage.png)
 
 ![MultiQC - Qualimap genomic origin plot](images/mqc_qualimap_features.png)