OMIM diseases as a function of associated HPO phenotypes. Data include
Por um escritor misterioso
Last updated 26 dezembro 2024
PDF] OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an
GPCards: An integrated database of genotype–phenotype correlations
Discovering Monogenic Patients with a Confirmed Molecular
Predicting disease-related phenotypes using an integrated
Figure 1 from The Human Phenotype Ontology project: linking
Linking common human diseases to their phenotypes; development of
Analysis of the human diseasome using phenotype similarity between
The Human Phenotype Ontology: A Tool for Annotating and Analyzing
Effective diagnosis of genetic disease by computational phenotype
Predicting missing associations in disease phenotype-gene
Common genetic variation associated with Mendelian disease
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