PhenoDis
PhenoDis is a manually annotated database providing symptomatic, genetic and imprinting information about rare cardiac diseases. PhenoDis is primarily concerned with the assignment of clinical symptoms to rare diseases using the biomedical literature as information source and the Human Phenotype Ontology (HPO) as vocabulary.
Description
More detailed information about this field from each metasource.
PhenoDis is a manually annotated database providing symptomatic, genetic and imprinting information about rare cardiac diseases. PhenoDis is primarily concerned with the assignment of clinical symptoms to rare diseases using the biomedical literature as information source and the Human Phenotype Ontology (HPO) as vocabulary.
metasource: Fairsharing.orgversion: FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Jan 03 2022 7:05 p.m.
Database for phenotypic characterization of rare cardiac diseases.
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:45.390298
Webpage:
http://mips.helmholtz-muenchen.de/phenodis/Webpage
More detailed information about this field from each metasource.
http://mips.helmholtz-muenchen.de/phenodis/
metasource: Fairsharing.orgversion: FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Jan 03 2022 7:05 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:45.390298
Licence:
Name: Helmholtz Zentrum Muenchen ImprintLicence name
More detailed information about this field from each metasource.
Helmholtz Zentrum Muenchen Imprint
metasource: Fairsharing.orgversion: FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Jan 03 2022 7:05 p.m.
Licence URL
More detailed information about this field from each metasource.
https://www.helmholtz-muenchen.de/en/imprint/index.html
metasource: Fairsharing.orgversion: FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Jan 03 2022 7:05 p.m.
Publications:
Publications
More detailed information about this field from each metasource.
PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases
PMID: 29370821
metasource: Fairsharing.org
version: FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Jan 03 2022 7:05 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:45.390298
Publications
More detailed information about this field from each metasource.
PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases
PMID: 29370821
metasource: Fairsharing.org
version: FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Jan 03 2022 7:05 p.m.
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:45.390298
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PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases
PubMed citations: 4.
4 articles citing: PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases
Data Sharing Under the General Data Protection Regulation: Time to Harmonize Law and Research Ethics? PMID:33583200
CancerLivER: a database of liver cancer gene expression resources and biomarkers. PMID:32147717
The utility of phenomics in diagnosis of inherited metabolic disorders. PMID:30651242
Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources. PMID:30476213
Tags:
Tags
More detailed information about this field from each metasource.
cardiovascular disease
metasource: Fairsharing.org
version: FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Jan 03 2022 7:05 p.m.
disease
metasource: Fairsharing.org
version: FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Jan 03 2022 7:05 p.m.
cardiology
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:45.390298
rare diseases
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:45.390298
personalised medicine
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:45.390298
Tags
More detailed information about this field from each metasource.
cardiovascular disease
metasource: Fairsharing.orgversion: FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Jan 03 2022 7:05 p.m.
disease
metasource: Fairsharing.orgversion: FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Jan 03 2022 7:05 p.m.
cardiology
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:45.390298
rare diseases
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:45.390298
personalised medicine
metasource: bio.toolsversion: extracted_at: 2022-11-04T11:30:45.390298
cardiovascular disease disease cardiology rare diseases personalised medicine
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