OMIM diseases as a function of associated HPO phenotypes. Data include
Por um escritor misterioso
Last updated 20 setembro 2024
Linking common human diseases to their phenotypes; development of
Deep phenotyping and whole‐exome sequencing improved the
Phenotype profile statistics for EQ-annotated OMIM genes
The Power of Being Counted – RARE-X
PhenCards: a data resource linking human phenotype information to
HPOSim: An R Package for Phenotypic Similarity Measure and
About - DECIPHER v11.23
PhenCards: a data resource linking human phenotype information to
HPO2Vec+: Leveraging heterogeneous knowledge resources to enrich
The Application of the Human Phenotype Ontology
Linking common human diseases to their phenotypes; development of
The pace of disease gene discovery as cataloged by the OMIM Morbid
Common genetic variation associated with Mendelian disease
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