Evidence map›Paper›PMID 40061308›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Consistent Performance of GPT-4o in Rare Disease Diagnosis Across Nine Languages and 4967 Cases.

Leonardo Chimirri, J Harry Caufield, Yasemin Bridges, Nicolas Matentzoglu, Michael Gargano, Mario Cazalla, Shihan Chen, Daniel Danis, Alexander Jm Dingemans, Petra Gehle and 19 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors.

Leonardo ChimirriBerlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID 0000-0002-6912-8518
J Harry CaufieldLawrence Berkeley National Laboratory, Berkeley, CA, USA.ORCID 0000-0001-5705-7831
Yasemin BridgesWilliam Harvey Research Institute, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.ORCID 0009-0002-1371-3782
Nicolas MatentzogluSemanticly, Athens, Greece.ORCID 0000-0002-7356-1779
Michael GarganoThe Jackson Laboratory for Genomic Medicine.ORCID 0000-0002-2157-3591
Mario CazallaINGEMM-Idipaz, Institute of Medical and Molecular Genetics, Hospital Universitario La Paz, Madrid, Spain.ORCID 0009-0007-1931-0390
Shihan ChenDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Daniel DanisBerlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID 0000-0003-0900-3411
Alexander Jm DingemansDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID 0000-0002-5648-2155
Petra GehleDeutsches Herzzentrum der Charité, Berlin, Germany.
Adam S L GraefeBerlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID 0009-0004-8124-8864
Weihong GuChinese HPO Consortium, Beijing, China.
Markus S LadewigDepartment of Ophthalmology, University Clinic Marburg - Campus Fulda, Fulda, Germany CIBERER-ISCIII, Madrid, Spain.ORCID 0000-0002-6601-4486
Pablo LapunzinaINGEMM-Idipaz, Institute of Medical and Molecular Genetics, Hospital Universitario La Paz, Madrid, Spain.ORCID 0000-0002-6324-4825
Julián NevadoINGEMM-Idipaz, Institute of Medical and Molecular Genetics, Hospital Universitario La Paz, Madrid, Spain.
Enock NiyonkuruLawrence Berkeley National Laboratory, Berkeley, CA, USA.
Soichi OgishimaINGEM/ToMMo, Tohoku University, Miyagi, Japan.ORCID 0000-0001-8613-2562
Dominik SeelowBerlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID 0000-0002-9746-4412
Jair A Tenorio CastañoINGEMM-Idipaz, Institute of Medical and Molecular Genetics, Hospital Universitario La Paz, Madrid, Spain.ORCID 0000-0002-5308-2316
Marek TurnovecDepartment of Biology and Medical Genetics, 2nd Faculty of Medicine, Charles University in Prague and Motol University Hospital, Prague, Czech Republic.ORCID 0000-0001-9497-3919
Bert Ba de VriesDepartment of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands.ORCID 0000-0002-0000-2917
Kai WangDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0002-5585-982X
Kyran WissinkBerlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID 0009-0007-8607-6506
Zafer YükselDepartment of Human Genetics, Bioscientia Healthcare GmbH, Ingelheim, Germany.ORCID 0000-0002-2085-5773
Gabriele ZuccaInstitute for Maternal and Child Health - IRCCS "Burlo Garofolo" - Trieste, Trieste 34137, Italy.ORCID 0000-0003-4174-0526
Melissa A HaendelUniversity of North Carolina at Chapel Hill.ORCID 0000-0001-9114-8737
Christopher J MungallLawrence Berkeley National Laboratory, Berkeley, CA, USA.ORCID 0000-0002-6601-2165
Justin ReeseLawrence Berkeley National Laboratory, Berkeley, CA, USA.ORCID 0000-0002-2170-2250
Peter N RobinsonBerlin Institute of Health at Charité - Universitätsmedizin Berlin, Berlin, Germany.ORCID 0000-0002-0736-9199

Funding

The Monarch Initiative: Linking Diseases to Model Organism ResourcesR24OD011883 · OD · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAENDEL, MELISSA A, MUNGALL, CHRISTOPHER J · 2012 to 2024
$16.0M
Improvements to the LinkML framework to support the Phenomics First open science resourceRM1HG010860 · NHGRI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI HAENDEL, MELISSA A, MUNGALL, CHRISTOPHER J · 2020 to 2024
$10.3M
The Human Phenotype Ontology: Accelerating Computational Integration of Clinical Data for GenomicsU24HG011449 · NHGRI · JACKSON LABORATORY · PI Peter Nicholas Robinson · 2021 to 2026
$6.7M
NHGRI NIH HHS RM1 HG010860NHGRI NIH HHS U24 HG011449NIH HHS R24 OD011883
6 · The paper itself

Abstract

Background: Large language models (LLMs) are increasingly used in the medical field for diverse applications including differential diagnostic support. The estimated training data used to create LLMs such as the Generative Pretrained Transformer (GPT) predominantly consist of English-language texts, but LLMs could be used across the globe to support diagnostics if language barriers could be overcome. Initial pilot studies on the utility of LLMs for differential diagnosis in languages other than English have shown promise, but a large-scale assessment on the relative performance of these models in a variety of European and non-European languages on a comprehensive corpus of challenging rare-disease cases is lacking. Methods: We created 4967 clinical vignettes using structured data captured with Human Phenotype Ontology (HPO) terms with the Global Alliance for Genomics and Health (GA4GH) Phenopacket Schema. These clinical vignettes span a total of 378 distinct genetic diseases with 2618 associated phenotypic features. We used translations of the Human Phenotype Ontology together with language-specific templates to generate prompts in English, Chinese, Czech, Dutch, German, Italian, Japanese, Spanish, and Turkish. We applied GPT-4o, version gpt-4o-2024-08-06, to the task of delivering a ranked differential diagnosis using a zero-shot prompt. An ontology-based approach with the Mondo disease ontology was used to map synonyms and to map disease subtypes to clinical diagnoses in order to automate evaluation of LLM responses. Findings: For English, GPT-4o placed the correct diagnosis at the first rank 19·8% and within the top-3 ranks 27·0% of the time. In comparison, for the eight non-English languages tested here the correct diagnosis was placed at rank 1 between 16·9% and 20·5%, within top-3 between 25·3% and 27·7% of cases. Interpretation: The differential diagnostic performance of GPT-4o across a comprehensive corpus of rare-disease cases was consistent across the nine languages tested. This suggests that LLMs such as GPT-4o may have utility in non-English clinical settings. Funding: NHGRI 5U24HG011449 and 5RM1HG010860. P.N.R. was supported by a Professorship of the Alexander von Humboldt Foundation; P.L. was supported by a National Grant (PMP21/00063 ONTOPRECISC-III, Fondos FEDER).

Identifiers

PMID40061308
PMCPMC11888497

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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.