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URL: http://www.human-phenotype-ontology.org/
Proper Citation: Human Phenotype Ontology (RRID:SCR_006016)
Description: 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.
Abbreviations: HPO, HP
Synonyms: Human Phenotype Ontology (HPO), Human Phenotype Ontology
Resource Type: controlled vocabulary, data or information resource, ontology
Defining Citation: PMID:20412080
Keywords: phenotype, genetics, disease, phenomizer, obo, clinical, phenome, pathological, organismal, FASEB list
Related Condition: Monogenic disease, Hereditary disease
Availability: Free, Freely available
Resource Name: Human Phenotype Ontology
Resource ID: SCR_006016
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Source: SciCrunch Registry (RRID:SCR_005400)
Description: Interactive portal for finding and submitting biomedical resources. Resources within SciCrunch have assigned RRIDs which are used to cite resources in scientific manuscripts. SciCrunch Registry, formerly NIF Registry, provides resources catalog. Allows to add new resources. Allows edit existing resources after registration. Curators are tasked with identifying and registering resources, examining data, writing configuration files to index and display data and keeping contents current.
URL: https://rrid.site/rin/sources/SCR_005400
The data sets included in this resource are published in Kravitz et al, 2012. Distinct roles for direct and indirect pathway striatal neurons in reinforcement (Nat. Neurosci).
