High-throughput phenotyping automates the mapping of patient signs to standardized concepts, such as those in Human Phenotype Ontology (HPO), a process critical to precision medicine. We evaluated the automated phenotyping of clinical summaries from the Online Mendelian Inheritance in Man (OMIM) database using a large language model. Various APIs were used to automate text retrieval, sign identification, categorization, and normalization. GPT-4 outperformed GPT-3.5Turbo in identifying, categorizing, and normalizing signs, achieving concordance with manual annotators comparable to concordance between manual annotators. While GPT-4 demonstrates high accuracy in sign identification and categorization, limitations remain in sign normalization, particularly in retrieving the correct HPO ID for a normalized term. Methods such as retrieval-augmented generation, changes in pre-training, and additional fine-tuning may help address these limitations. The combination of APIs with large language models presents a promising approach for high-throughput phenotyping of free text.
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