# RareGraph-Synth: Knowledge-Guided Diffusion Models for Generating Privacy-Preserving Synthetic Patient Trajectories in Ultra-Rare Diseases

arXiv: https://arxiv.org/abs/2510.06267 · HTML: https://mlsanity.com/paper/2510.06267/

## Key facts

- No citing papers in the map yet (data through 14 Oct 2026).
- Placed in Medical imaging and segmentation, one of 14 directions in Diffusion models.
- Builds on 6 of its 29 references that are in the map.
- First posted on arXiv 6 Oct 2025.

## Placed in

- Diffusion models / [Medical imaging and segmentation](https://mlsanity.com/diffusion/medical-imaging-and-segmentation/)

## Builds on (most cited first, 6 of 6)

- [Denoising Diffusion Probabilistic Models](https://mlsanity.com/paper/2006.11239/) (2020)
- [Score-Based Generative Modeling through Stochastic Differential Equations](https://mlsanity.com/paper/2011.13456/) (2020)
- [Membership Inference Attacks against Machine Learning Models](https://mlsanity.com/paper/1610.05820/) (2016)
- [Modeling Tabular data using Conditional GAN](https://mlsanity.com/paper/1907.00503/) (2019)
- [Wasserstein GAN](https://mlsanity.com/paper/1701.07875/) (2017)
- [How Faithful is your Synthetic Data? Sample-level Metrics for Evaluating and Auditing Generative Models](https://mlsanity.com/paper/2102.08921/) (2021)

## Abstract (arXiv)

We propose RareGraph-Synth, a knowledge-guided, continuous-time diffusion framework that generates realistic yet privacy-preserving synthetic electronic-health-record (EHR) trajectories for ultra-rare diseases. RareGraph-Synth unifies five public resources: Orphanet/Orphadata, the Human Phenotype Ontology (HPO), the GARD rare-disease KG, PrimeKG, and the FDA Adverse Event Reporting System (FAERS) into a heterogeneous knowledge graph comprising approximately 8 M typed edges. Meta-path scores extracted from this 8-million-edge KG modulate the per-token noise schedule in the forward stochastic differential equation, steering generation toward biologically plausible lab-medication-adverse-event co-occurrences while retaining score-based diffusion model stability. The reverse denoiser then produces timestamped sequences of lab-code, medication-code, and adverse-event-flag triples that contain no protected health information. On simulated ultra-rare-disease cohorts, RareGraph-Synth lowers categorical Maximum Mean Discrepancy by 40 percent relative to an unguided diffusion baseline and by greater than 60 percent versus GAN counterparts, without sacrificing downstream predictive utility. A black-box membership-inference evaluation using the DOMIAS attacker yields AUROC approximately 0.53, well below the 0.55 safe-release threshold and substantially better than the approximately 0.61 plus or minus 0.03 observed for non-KG baselines, demonstrating strong resistance to re-identification. These results suggest that integrating biomedical knowledge graphs directly into diffusion noise schedules can simultaneously enhance fidelity and privacy, enabling safer data sharing for rare-disease research.