OMIM diseases as a function of associated HPO phenotypes. Data include
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Predicting disease-related phenotypes using an integrated
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Figure 1 from The Human Phenotype Ontology project: linking
HPOSim: An R Package for Phenotypic Similarity Measure and
Combining exome/genome sequencing with data repository analysis
Curation and expansion of Human Phenotype Ontology for defined
PhenCards: a data resource linking human phenotype information to
Phenotype-aware prioritisation of rare Mendelian disease variants
Phenotype profile statistics for EQ-annotated OMIM genes
OMIM diseases as a function of associated HPO phenotypes. Data
PhenoExam: an R package and Web application for the examination of
HPO2Vec+: Leveraging heterogeneous knowledge resources to enrich
Curation and expansion of Human Phenotype Ontology for defined
Predicting disease-related phenotypes using an integrated
Human genotype–phenotype databases: aims, challenges and
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