HPO specifications

Unique identifier:
OMICS_10079
Restrictions to use:
None
Name:
Human Phenotype Ontology
Maintained:
Yes
  • Animals
    • Homo sapiens

HPO support

Documentation

Maintainer

  • Peter N. Robinson <>

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Publications

Institution(s)

Institute for Medical Genetics and Human Genetics, Charité-Universitätsmedizin Berlin, Berlin, Germany; Berlin-Brandenburg Center for Regenerative Therapies, Charite-Universita tsmedizin Berlin, Berlin, Germany; [etc]

Funding source(s)

National Institutes of Health (NIH) Monarch Initiative [NIH OD #5R24OD011883]; E-RARE 2015 program, Hipbi-RD (harmonizing phenomics information for a better interoperability in the RD field); Director, Office of Science, Office of Basic Energy Sciences, of the U.S. Department of Energy under [DE-AC02-05CH11231]; Bundesministerium für Bildung und Forschung (BMBF) [0313911]; Raine Clinician Research Fellowship; Stanley Institute for Cognitive Genomics at Cold Spring Harbor Laboratory (CSHL); European Union Seventh Framework Programme [FP7/2007-2013] supported RD-Connect [305444], EURenOmics [2012-305608] and NeurOmics [2012-305121]; Fight for Sight and Retinitis Pigmentosa Fighting Blindness; National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital National Health Service Foundation Trust and UCL Institute of Ophthalmology (UK); University of Kiel, by a grant from the German Research Foundation [HE5415/3-1] within the EuroEPINOMICS framework of the European Science Foundation and grants of the German Research Foundation [DFG, HE5415/5-1, HE5415/6-1], German Ministry for Education and Research [01DH12033, MAR 10/012] and by the German chapter of the International League against Epilepsy (DGfE); International League Against Epilepsy (ILAE) within the Epilepsiome initiative of the ILAE Genetics Commission (www.channelopathist.net); National Library of Medicine [R44 LM011585-02]; the Dutch Organisation for Health Research and Development (ZON-MW grants 912-12-109)

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