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Digital medicine Outcomes Value Set (DOVeS) Ontology
Last uploaded:
December 13, 2023
Acronym | DOVES |
Visibility | Public |
Description | The Digital medicine Outcomes Value Set (DOVeS) ontology aims to provide users with a set of ontologically structured healthcare outcomes (clinical, operational, economic, technical, and others) tailored to digital medicine and digital therapeutic applications. |
Status | Alpha |
Format | OWL |
Contact | Benjamin Rosner, benjamin.rosner@uscf.edu Matthew Horridge, horridge@stanford.edu |
Categories | Health, Human |
Version | Released | Uploaded | Downloads |
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releases/2023-03-01 (Parsed, Indexed, Metrics, Annotator) | 12/13/2023 | 12/13/2023 | OWL | CSV | RDF/XML |
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Id | http://purl.obolibrary.org/obo/MONDO_0010726
http://purl.obolibrary.org/obo/MONDO_0010726
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Preferred Name | Rett syndrome |
Definitions |
A severe neurodevelopmental disorder affecting the central nervous system.
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Synonyms |
RTT
Rts
Rett syndrome, atypical
Rett syndrome, Zappella variant
Rett syndrome, preserved speech variant
autism, dementia, ataxia, and loss of purposeful hand use
rett syndrome, preserved speech variant, X-linked dominant
Rett's disorder
Rett syndrome
rett syndrome, X-linked dominant
rett syndrome, atypical, X-linked dominant
cerebroatrophic hyperammonemia
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Type | http://www.w3.org/2002/07/owl#Class |
All Properties
definition | A severe neurodevelopmental disorder affecting the central nervous system. |
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altLabel |
RTT
Rts
Rett syndrome, atypical
Rett syndrome, Zappella variant
Rett syndrome, preserved speech variant
autism, dementia, ataxia, and loss of purposeful hand use
rett syndrome, preserved speech variant, X-linked dominant
Rett's disorder
Rett syndrome
rett syndrome, X-linked dominant
rett syndrome, atypical, X-linked dominant
cerebroatrophic hyperammonemia
See more
See less
|
label | Rett syndrome
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prefLabel | Rett syndrome
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IAO_0000233 | |
has_related_synonym |
RTT
Rts
Rett syndrome, atypical
Rett syndrome, Zappella variant
Rett syndrome, preserved speech variant
autism, dementia, ataxia, and loss of purposeful hand use
See more
See less
|
disease has feature | |
prefixIRI | MONDO:0010726
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textual definition | A severe neurodevelopmental disorder affecting the central nervous system.
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subClassOf | |
type | |
has_exact_synonym |
rett syndrome, preserved speech variant, X-linked dominant
Rett's disorder
Rett syndrome
rett syndrome, X-linked dominant
rett syndrome, atypical, X-linked dominant
cerebroatrophic hyperammonemia
See more
See less
|
has characteristic |
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Add NCBO Web Widgets to your site for DOVES
Widget type | Widget demonstration |
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Step 2: Follow the Instructions
For more help visit NCBO Widget Wiki |
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Example 1 (start typing the class name to get its full URI)
Example 2 (get the ID for a class) Example 3 (get the preferred name for a class) Step 2: Follow the Instructions
For more help visit NCBO Widget Wiki |
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Step 2: Follow the InstructionsCopy the code below and paste it to your HTML page <iframe frameborder="0" src="/widgets/visualization?ontology=DOVES&class=http%3A%2F%2Fpurl.obolibrary.org%2Fobo%2FMONDO_0044647&apikey=YOUR_API_KEY"></iframe> For more help visit NCBO Widget Wiki |
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Step 2: Follow the InstructionsCopy the code below and paste it to your HTML page <link rel="stylesheet" type="text/css" href="/widgets/jquery.ncbo.tree.css"> <script src="/widgets/jquery.ncbo.tree-2.0.2.js"></script> <div id="widget_tree"></div> var widget_tree = $("#widget_tree").NCBOTree({ apikey: "YOUR_API_KEY", ontology: "DOVES" }); You can also view a detailed demonstration For more help visit NCBO Widget Wiki |