CONAN: Complementary Pattern Augmentation for Rare Disease Detection
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Abstract (arXiv)
Rare diseases affect hundreds of millions of people worldwide but are hard to detect since they have extremely low prevalence rates (varying from 1/1,000 to 1/200,000 patients) and are massively underdiagnosed. How do we reliably detect rare diseases with such low prevalence rates? How to further leverage patients with possibly uncertain diagnosis to improve detection? In this paper, we propose a Complementary pattern Augmentation (CONAN) framework for rare disease detection. CONAN combines ideas from both adversarial training and max-margin classification. It first learns self-attentive and hierarchical embedding for patient pattern characterization. Then, we develop a complementary generative adversarial networks (GAN) model to generate candidate positive and negative samples from the uncertain patients by encouraging a max-margin between classes. In addition, CONAN has a disease detector that serves as the discriminator during the adversarial training for identifying rare diseases. We evaluated CONAN on two disease detection tasks. For low prevalence inflammatory bowel disease (IBD) detection, CONAN achieved .96 precision recall area under the curve (PR-AUC) and 50.1% relative improvement over best baseline. For rare disease idiopathic pulmonary fibrosis (IPF) detection, CONAN achieves .22 PR-AUC with 41.3% relative improvement over the best baseline.
Key facts. Cited by 9 papers in the map (data through 14 Oct 2026). First posted on arXiv 26 Nov 2019.
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Citing papers per year: 2021: 1; 2022: 2; 2023: 2; 2024: 1; 2025: 3.
9 papers.
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- 2022Artificial Intelligence for In Silico Clinical Trials: A Reviewcited by 6
- 2023Collaborative Synthesis of Patient Records through Multi-Visit Health State Inferencecited by 6
- 2025Generating Clinically Realistic EHR Data via a Hierarchy- and Semantics-Guided Transformercited by 4
- 2025CEHR-XGPT: A Scalable Multi-Task Foundation Model for Electronic Health Recordscited by 4
- 2021Machine Learning Applications for Therapeutic Tasks with Genomics Datacited by 3
- 2024Fairness-Optimized Synthetic EHR Generation for Arbitrary Downstream Predictive Taskscited by 1
- 2025Knowledge Graph Sparsification for GNN-based Rare Disease Diagnosiscited by 0
- 2025Knowledge Graph Sparsification for GNN-based Rare Disease Diagnosis9 Oct 2025
- 2025CEHR-XGPT: A Scalable Multi-Task Foundation Model for Electronic Health Records3 Sep 2025
- 2025Generating Clinically Realistic EHR Data via a Hierarchy- and Semantics-Guided Transformer28 Feb 2025
- 2024Fairness-Optimized Synthetic EHR Generation for Arbitrary Downstream Predictive Tasks4 Jun 2024
- 2023Collaborative Synthesis of Patient Records through Multi-Visit Health State Inference22 Dec 2023
- 2023Synthesize High-dimensional Longitudinal Electronic Health Records via Hierarchical Autoregressive Language Model4 Apr 2023
- 2022PromptEHR: Conditional Electronic Healthcare Records Generation with Prompt Learning11 Oct 2022
- 2022Artificial Intelligence for In Silico Clinical Trials: A Review16 Sep 2022
- 2021Machine Learning Applications for Therapeutic Tasks with Genomics Data3 May 2021