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SciCrunch Registry is a curated repository of scientific resources, with a focus on biomedical resources, including tools, databases, and core facilities - visit SciCrunch to register your resource.

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Resource Name Proper Citation Abbreviations Resource Type Description Keywords Resource Relationships Related Condition Funding Defining Citation Availability Specification URL Alternate IDs Alternate URLs Old URLs Parent Organization Resource ID Synonyms Record Last Update Mentions Count
Phenexplorer
 
Resource Report
Resource Website
1+ mentions
Phenexplorer (RRID:SCR_006156) PhenExplorer service resource, analysis service resource, data or information resource, database, data analysis service, production service resource The PhenExplorer allows you to browse the Human Phenotype Ontology (HPO) in different ways, using the tabs ''''by features'''', ''''by disease'''', ''''by ontology'''' or ''''by genes''''. Clicking on a particular phenotypic feature (HPO-term) you can get a list of disease entries that are linked to it (i.e. diseases that are annotated with this HPO-term). You can also visualize this term in the context of the ontological structure. Finally, a lists of genes can be displayed, that are known to cause (when mutated) the linked diseases mentioned above. For each disease you can get the list of linked HPO-terms and genes. You can also search for specific genes and explore to which HPO-terms and diseases they are linked. phenotype, ontology, feature, disease, gene is used by: Human Phenotype Ontology
is related to: Human Phenotype Ontology
has parent organization: Charite - Universitatsmedizin Berlin; Berlin; Germany
nlx_151656 SCR_006156 PhenExplorer - Explore the Human Phenotype Ontology 2026-08-11 09:41:22 2
Charite - Universitatsmedizin Berlin; Berlin; Germany
 
Resource Report
Resource Website
1+ mentions
Charite - Universitatsmedizin Berlin; Berlin; Germany (RRID:SCR_011151) Charite, Charité university One of Europe's largest university hospitals, affiliated with Humboldt University and Free University Berlin. With numerous Collaborative Research Centres of the German Research Foundation it is one of Germany's most research-intensive medical institutions. is related to: OncoTrack
is related to: ONE Study
has parent organization: Free University of Berlin; Berlin; Germany
has parent organization: Humboldt University of Berlin; Berlin; Germany
is parent organization of: HOMOZYGOSITYMAPPER
is parent organization of: SuperPred: Drug classification and target prediction
is parent organization of: SuperTarget
is parent organization of: LEAD-DBS
is parent organization of: SynSysNet
is parent organization of: Ontologizer
is parent organization of: Human Phenotype Ontology
is parent organization of: Phenexplorer
is parent organization of: Phenomizer
is parent organization of: CellFinder
is parent organization of: GraphVar: A toolbox for comprehensive graph analyses of functional brain connectivity
is parent organization of: monoclonal antibody-based chemiluminescence immunoassay for 3,5-diiodothyronine (3,5-T2)
is parent organization of: Trial Registration Number screener
is parent organization of: International Graduate Program Medical Neurosciences
is parent organization of: Charite University and Berlin Institute for Health Research Central Biobank Core Facility
is parent organization of: Charité Berlin University of Medicine Transgenic Technologies Core Facility
is parent organization of: Charité Berlin University of Medicine Cryo-Electron Microscopy Core Facility
is parent organization of: Charité Berlin University of Medicine Virchow Clinic Campus Experimental Hybrid Operating Room Core Facility
is parent organization of: Charité Berlin University of Medicine Viral Core Facility
is parent organization of: Charité Berlin University of Medicine iPATH.Berlin Core Facility
is parent organization of: Charité Berlin University of Medicine Animal Behavior Phenotyping Core Facility
is parent organization of: Charité Berlin University Medicine Research Institutes for Experimental Medicine Core Facility
is parent organization of: Charité Berlin University of Medicine Advanced Medical Bioimaging Core Facility
is parent organization of: Berlin Center for Advanced Neuroimaging Core Facility
is parent organization of: Charité Berlin University of Medicine Central Radionuclide Laboratory Core Facility
is parent organization of: Charité Berlin University of Medicine Scientific Workshop Core Facility
is parent organization of: Charité Berlin University of Medicine Electron Microscopy Core Facility
is parent organization of: Charite Berlin University of Medicine Berlin Experimental Radionuclide Imaging Center BERIC Core Facility
GRID grid.6363.0, Crossref Funder ID 501100002839, ISNI 0000 0001 2218 4662, nlx_149288, Wikidata Q162684 https://ror.org/001w7jn25 SCR_011151 , Charité - University Medicine Berlin, Charite - Universitatsmedizin Berlin, Charite Universitatsmedizin Berlin, Charité University of Medicine, Charité Berlin University of Medicine, Charite - University Medicine Berlin; Berlin; Germany, Charité Universitätsmedizin Berlin, Charite - University Medicine Berlin, Charite University of Medicine, Charité - Universitätsmedizin Berlin 2026-08-08 11:59:43 7
Human Phenotype Ontology
 
Resource Report
Resource Website
50+ mentions
Human Phenotype Ontology (RRID:SCR_006016) HPO, HP data or information resource, controlled vocabulary, ontology Provides standardized vocabulary of phenotypic abnormalities encountered in human disease. Structured and controlled vocabulary for phenotypic features encountered in human hereditary and other disease. HPO is being developed in collaboration with members of OBO Foundry (Open Biological and Biomedical Ontologies), and logical definitions for HPO terms are being developed using PATO and a number of other ontologies including FMA, GO, ChEBI, and MPATH. phenotype, genetics, disease, phenomizer, obo, clinical, phenome, pathological, organismal, FASEB list uses: OMIM
uses: Phenexplorer
is used by: DisGeNET
is used by: HmtPhenome
is used by: MONARCH Initiative
is used by: NIF Data Federation
is listed by: BioPortal
is listed by: OBO
is related to: Phenexplorer
is related to: Phenomizer
is related to: PhenoTips
is related to: Neurocarta
is related to: GWASdb
is related to: Phenomizer
has parent organization: Charite - Universitatsmedizin Berlin; Berlin; Germany
works with: Human Mouse Disease Connection
Monogenic disease, Hereditary disease PMID:20412080 Free, Freely available SCR_006219, nlx_151406, nlx_151835 http://purl.bioontology.org/ontology/HP, http://compbio.charite.de/svn/hpo/trunk/src/ontology/human-phenotype-ontology.obo SCR_006016 Human Phenotype Ontology (HPO), Human Phenotype Ontology 2026-08-11 09:41:21 76

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