databases > DOI:10.25504/FAIRsharing.FwFGGF
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ready PhenoDis

General Information
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.

Homepage http://mips.helmholtz-muenchen.de/phenodis/

Countries that developed this resource Germany

Created in 2017

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How to cite this record FAIRsharing.org: PhenoDis; PhenoDis; DOI: https://doi.org/10.25504/FAIRsharing.FwFGGF; Last edited: Dec. 19, 2019, 11:06 a.m.; Last accessed: Sep 23 2020 12:01 a.m.

Publication for citation  PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases. Adler A,Kirchmeier P,Reinhard J,Brauner B,Dunger I,Fobo G,Frishman G,Montrone C,Mewes HW,Arnold M,Ruepp A; Orphanet J Rare Dis ; 2018; 10.1186/s13023-018-0765-y;


This record is maintained by AndreasRuepp

Record added: Oct. 1, 2019, 1:25 p.m.
Record updated: Oct. 1, 2019, 1:41 p.m. by The FAIRsharing Team.

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PhenoDis: a comprehensive database for phenotypic characterization of rare cardiac diseases.

Adler A,Kirchmeier P,Reinhard J,Brauner B,Dunger I,Fobo G,Frishman G,Montrone C,Mewes HW,Arnold M,Ruepp A
Orphanet J Rare Dis 2018

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