Artificial Intelligence System for Diagnosing Rare Diseases: Design Principles and Clinical Validation Results

Introduction. Differential diagnostics of rare diseases at the pre-laboratory stage of patient examination is a significant challenge not only for pediatricians but also for geneticists. This fact is caused by limited physician experience in managing rare diseases, variability in symptom presentation, and ambiguity of clinical signs. AI-driven clinical decision support systems (CDSS) enable the generation and validation of diagnostic hypotheses. Aim: To assess the architecture of the GenDiES (Genetic Diagnostic Expert System) CDSS for differential diagnosis of lysosomal storage diseases (LSDs) at the pre-laboratory stage and to present results from its clinical validation. Material and Methods. The study included 30 clinical forms of LSDs, described using 35 clinical features based on three complementary expert-derived metrics: modality coefficient (diagnostic importance), manifestation certainty factor, and degree of expression certainty factor. Knowledge was extracted from literature and refined through expert input, where experts assigned their confidence to each feature across four age groups: ≤ 1 year, 1–3 years, 4–6 years, ≥ 7 years. This structured data formed the system’s knowledge base. Clinical aprobation utilized de-identified electronic health records (EHR) of pediatric LSD patients (mucopolysaccharidoses, mucolipidoses, gangliosidoses-conditions with broad overlapping phenotypic spectra). Validation cohort: 54 EHR extracts from a single Russian medical institution. Verification cohort: 38 EHR extracts from three institutions across different Russian regions. The system was built using knowledge engineering methods (for knowledge extraction and structuring), a matrix-based framework (to organize rules), and custom software for implementation. Results. The updated GenDiES CDSS for differential diagnosis of rare hereditary diseases was deployed as a web application. Its knowledge base contains 12,600 expert confidence assessments for 35 clinical features across 30 LSD subtypes, categorized by age. A similarity-based algorithm compares patient profiles to expert-defined disease patterns. Accuracy for generating a differential diagnosis shortlist (top five hypotheses) reached 0.87 (95% CI [0.75; 0.95]) during validation and 0.90 (95% CI [0.75; 0.97]) during verification. Conclusion. The GenDiES system demonstrated high diagnostic accuracy at the pre-laboratory stage, comparable to—and in some cases exceeding—the performance of limited existing international counterparts. Its web-based implementation ensures accessibility for physicians via any internet-connected device.

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Publication Details

Journal
Siberian Journal of Clinical and Experimental Medicine
Published
2025-06-11
DOI
https://doi.org/10.29001/2073-8552-2025-2706
Primary Topic
Genomics and Rare Diseases
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article
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article

Artificial Intelligence System for Diagnosing Rare Diseases: Design Principles and Clinical Validation Results

Н. А. Благосклонов, Б. А. Кобринский
Siberian Journal of Clinical and Experimental Medicine
Genomics and Rare Diseases
article

Artificial Intelligence System for Diagnosing Rare Diseases: Design Principles and Clinical Validation Results

Н. А. Благосклонов, Б. А. Кобринский
article en

Abstract

Introduction. Differential diagnostics of rare diseases at the pre-laboratory stage of patient examination is a significant challenge not only for pediatricians but also for geneticists. This fact is caused by limited physician experience in managing rare diseases, variability in symptom presentation, and ambiguity of clinical signs. AI-driven clinical decision support systems (CDSS) enable the generation and validation of diagnostic hypotheses. Aim: To assess the architecture of the GenDiES (Genetic Diagnostic Expert System) CDSS for differential diagnosis of lysosomal storage diseases (LSDs) at the pre-laboratory stage and to present results from its clinical validation. Material and Methods. The study included 30 clinical forms of LSDs, described using 35 clinical features based on three complementary expert-derived metrics: modality coefficient (diagnostic importance), manifestation certainty factor, and degree of expression certainty factor. Knowledge was extracted from literature and refined through expert input, where experts assigned their confidence to each feature across four age groups: ≤ 1 year, 1–3 years, 4–6 years, ≥ 7 years. This structured data formed the system’s knowledge base. Clinical aprobation utilized de-identified electronic health records (EHR) of pediatric LSD patients (mucopolysaccharidoses, mucolipidoses, gangliosidoses-conditions with broad overlapping phenotypic spectra). Validation cohort: 54 EHR extracts from a single Russian medical institution. Verification cohort: 38 EHR extracts from three institutions across different Russian regions. The system was built using knowledge engineering methods (for knowledge extraction and structuring), a matrix-based framework (to organize rules), and custom software for implementation. Results. The updated GenDiES CDSS for differential diagnosis of rare hereditary diseases was deployed as a web application. Its knowledge base contains 12,600 expert confidence assessments for 35 clinical features across 30 LSD subtypes, categorized by age. A similarity-based algorithm compares patient profiles to expert-defined disease patterns. Accuracy for generating a differential diagnosis shortlist (top five hypotheses) reached 0.87 (95% CI [0.75; 0.95]) during validation and 0.90 (95% CI [0.75; 0.97]) during verification. Conclusion. The GenDiES system demonstrated high diagnostic accuracy at the pre-laboratory stage, comparable to—and in some cases exceeding—the performance of limited existing international counterparts. Its web-based implementation ensures accessibility for physicians via any internet-connected device.

Siberian Journal of Clinical and Experimental MedicineVol. 40(2)
Russian Academy of Sciences (RU), Pirogov Russian National Research Medical University (RU)
Peace, Justice and strong institutions
Openalex Percentile: Top 85%
Genomics and Rare Diseases
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