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Paper Details

Rare disease knowledge enrichment through a data-driven approach.
BMC Med Inform Decis Mak
15
2019
EMR, HPO, Hodgkin lymphoma, Human, Rare disease, rare, rare disease
Algorithms, Data Mining, Electronic Health Records, Humans, Knowledge Bases, Phenotype, Rare Diseases
Author NameAffiliation
Feichen ShenMayo Clinic
Yiqing ZhaoMayo Clinic
Liwei WangMayo Clinic
Majid Rastegar-MojaradMayo Clinic
Yanshan WangMayo Clinic
Sijia LiuMayo Clinic
Hongfang LiuMayo Clinic
Hongfang LiuMayo Clinic
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Datasets

Dataset
Description
Source Link
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Human Phenotype OntologyStandardized vocabulary of phenotypic abnormalities in human diseaseLink
Release 1.2