OMIM diseases as a function of associated HPO phenotypes. Data include
Por um escritor misterioso
Last updated 02 junho 2024
The pace of disease gene discovery as cataloged by the OMIM Morbid
HPOSim: An R Package for Phenotypic Similarity Measure and
Linking common human diseases to their phenotypes; development of
Encoding Clinical Data with the Human Phenotype Ontology for
Getting started with the rare disease database: OMIM
Best practices for the interpretation and reporting of clinical
Curation and expansion of Human Phenotype Ontology for defined
VarfromPDB: An Automated and Integrated Tool to Mine Disease-Gene
Genes, Free Full-Text
Matching whole genomes to rare genetic disorders: Identification
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