OMIM diseases as a function of associated HPO phenotypes. Data include
Por um escritor misterioso
Last updated 26 dezembro 2024
Phenotype-loci associations in networks of patients with rare
Genes, Free Full-Text
Getting started with the rare disease database: OMIM
Deep phenotyping and whole‐exome sequencing improved the
The Application of the Human Phenotype Ontology
Common genetic variation associated with Mendelian disease
PhenoExam: an R package and Web application for the examination of
Getting started with the rare disease database: OMIM
About - DECIPHER v11.23
The Application of the Human Phenotype Ontology
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