OMIM diseases as a function of associated HPO phenotypes. Data include
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HPO2Vec+: Leveraging heterogeneous knowledge resources to enrich
Frontiers Gene- and Disease-Based Expansion of the Knowledge on
About - DECIPHER v11.23
The Human Phenotype Ontology: Semantic Unification of Common and
OMIM diseases as a function of associated HPO phenotypes. Data
Figure 1 from OMIM.org: Online Mendelian Inheritance in Man (OMIM
Screening genes of the panel. HGMD, Human Gene Mutation Database
Computational Methods for Identifying Similar Diseases: Molecular
Figure 2 from OMIM.org: Online Mendelian Inheritance in Man (OMIM
Getting started with the rare disease database: OMIM
Discovering Monogenic Patients with a Confirmed Molecular
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por adulto (o preço varia de acordo com o tamanho do grupo)
