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Resource Name
RRID:SCR_006016 RRID Copied      
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Human Phenotype Ontology (RRID:SCR_006016)
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Resource Information

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: ontology, controlled vocabulary, data or information resource

Defining Citation: PMID:20412080

Keywords: phenotype, genetics, disease, phenomizer, obo, clinical, phenome, pathological, organismal, FASEB list

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This resource

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

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