Evidence map›Paper›PMID 40776018›Full record

ArticleStudies in health technology and informatics2025

Accuracy of Large Language Models in Generating Rare Disease Differential Diagnosis Using Key Clinical Features.

Cathy Shyr, Rory J Tinker, Paul A Harris, Alex C Cheng, Kevin W Byram, Lisa Bastarache, Josh F Peterson, Rizwan Hamid, Hua Xu, Thomas A Cassini

Abstract read
In one paragraph

Article in Studies in health technology and informatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Cathy ShyrDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.
Rory J TinkerDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
Paul A HarrisDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.
Alex C ChengDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.
Kevin W ByramDepartment of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
Lisa BastaracheDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.
Josh F PetersonDepartment of Biomedical Informatics, Vanderbilt University Medical Center, Nashville, TN, USA.
Rizwan HamidDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.
Hua XuDepartment of Biomedical Informatics and Data Science, Yale School of Medicine, New Haven, CT, USA.
Thomas A CassiniDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, TN, USA.

Funding

Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Lea K Davis · 2020 to 2026
$10.3M
Vanderbilt Center of Excellence for Undiagnosed Disease (VCEUD)U01NS134349 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI JOY D COGAN, Thomas Anthony Cassini · 2023 to 2026
$3.8M
Development and implementation of statistical machine learning methods to shorten rare disease odysseysR00LM014429 · NLM · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Cathy Shyr · 2025 to 2026
$493k
Development and implementation of statistical machine learning methods to shorten rare disease odysseysK99LM014429 · NLM · VANDERBILT UNIVERSITY MEDICAL CENTER · PI SHYR, CATHY · 2024 to 2025
$181k
NICHD NIH HHS P50 HD103537NINDS NIH HHS U01 NS134349NLM NIH HHS K99 LM014429NLM NIH HHS R00 LM014429
6 · The paper itself

Abstract

Generating differential diagnoses for rare disease patients can be time intensive and highly dependent on the background and training of the evaluating physicians. Large language models (LLMs) have the potential to complement this process by automatically generating differentials to support physicians, but their performance in real-world patient populations remains underexplored. To this end, we assessed the diagnostic accuracy of ChatGPT-4o, Llama 3.1-8B-Instruct, and Exomiser in 424 rare disease patients at the Undiagnosed Diseases Network. ChatGPT-4o had the highest differential diagnostic accuracy (22.4% [95% CI: 18.4, 26.4]), outperforming Exomiser (13.9% [10.6, 17.2]; p < 0.001) and Llama 3.1-8B-Instruct (11.6% [8.5, 14.6]; p < 0.001). Adjusting for other factors, age at symptom onset was a significant predictor of ChatGPT-4o's diagnostic accuracy with the model performing better in patients with later symptom onset, potentially due to more distinct phenotypic presentations in older individuals. The combined accuracy of ChatGPT-4o and Exomiser was 30% [25.6, 34.3] and higher than that of either model alone (p < 0.01). This improvement highlights the potential of combining LLMs and bioinformatic models to generate differential diagnoses for rare diseases.

Indexed as

Diagnosis, Computer-AssistedNatural Language ProcessingRare DiseasesDiagnosis, DifferentialFemaleHumansLarge Language ModelsMaledifferential diagnosisExomiserlarge language modelsRare disease

Identifiers

PMID40776018
PMCPMC13075642

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.