FINDbase specifications

Unique identifier:
Restrictions to use:
Data access:
Frequency of INherited Disorders database
Community driven:
User data submission:
  • Animals
    • Homo sapiens

FINDbase support


  • George Patrinos <>


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University of Patras, Faculty of Engineering, Department of Computer Engineering and Informatics, Patras, Greece; Department of Pharmacy, School of Health Sciences, University of Patras, Patras, Greece; Erasmus University Medical Center, Faculty of Medicine and Health Sciences, Department of Bioinformatics, Rotterdam, The Netherlands; University of Malta, Faculty of Medicine and Surgery, Department of Physiology and Biochemistry, Malta; Institute of Molecular Genetics and Genetic Engineering, University of Belgrade, Laboratory of Molecular Biomedicine, Belgrade, Serbia; The Golden Helix Foundation, London, UK; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland; Department of Experimental Medical Science, Lund University, Lund, Sweden; Department of Computer and Informatics Engineering, Technological Educational Institute of Western Greece, Patras, Greece

Funding source(s)

Supported by European Commission [GEN2PHEN (FP7-200754), RDCONNECT (FP7-305444), SEE DRUG (FP7-285950), UPGx (H2020-668353) and SERBORDISInn (FP7-316088)]; Greek State grant [EAvEK 2014- 2020; ELIXIR GR)]; Serbian State grant [III 41004 MESTD RS] and Golden Helix Foundation (UK).

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