OMIM diseases as a function of associated HPO phenotypes. Data include
Por um escritor misterioso
Last updated 16 julho 2024
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Computational Methods for Identifying Similar Diseases: Molecular
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Linking common human diseases to their phenotypes; development of
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Genes, Free Full-Text
![OMIM diseases as a function of associated HPO phenotypes. Data include](https://www.cell.com/cms/attachment/756ed61a-c3a4-4b00-8a2c-8e86a3b76df3/gr1_lrg.jpg)
Phenotype-aware prioritisation of rare Mendelian disease variants
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Predicting disease-related phenotypes using an integrated
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Getting started with the rare disease database: OMIM
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PhenCards: a data resource linking human phenotype information to
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Summary of diseases found in OMIM and Orphanet databases and the
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MouseFinder: Candidate disease genes from mouse phenotype data
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Clinical phenotype-based gene prioritization: an initial study
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Encoding Clinical Data with the Human Phenotype Ontology for
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