OMIM diseases as a function of associated HPO phenotypes. Data include
Por um escritor misterioso
Last updated 18 maio 2024
Text mining of gene–phenotype associations reveals new phenotypic
PhenoExam: an R package and Web application for the examination of
HPOSim: An R Package for Phenotypic Similarity Measure and
The Application of the Human Phenotype Ontology
New models for human disease from the International Mouse
JPM, Free Full-Text
The Human Phenotype Ontology: A Tool for Annotating and Analyzing
About - DECIPHER v11.23
Integrative Data Mining Highlights Candidate Genes for Monogenic
Deep learning for diagnosing patients with rare genetic diseases
PDF] OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an
Phenotype-loci associations in networks of patients with rare
Genes, Free Full-Text
Figure 2 from OMIM.org: Online Mendelian Inheritance in Man (OMIM
Linking common human diseases to their phenotypes; development of
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