BioAssay Ontology

Last uploaded: February 21, 2024
Preferred Name

hereditary night blindness
Synonyms

Congenital night blindness

Definitions

OMIM mapping confirmed by DO. [SN].

ID

http://purl.obolibrary.org/obo/DOID_8498

comment

OMIM mapping confirmed by DO. [SN].

database_cross_reference

ICD9CM:368.61

MESH:C537743

UMLS_CUI:C1306122

ICD10CM:H53.63

SNOMEDCT_US_2020_03_01:193687000

has exact synonym

Congenital night blindness

has_obo_namespace

disease_ontology

id

DOID:8498

imported from

http://purl.obolibrary.org/obo/doid.owl

label

hereditary night blindness

notation

DOID:8498

prefLabel

hereditary night blindness

subClassOf

http://purl.obolibrary.org/obo/DOID_8499

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The BioAssay Ontology integrates with OntoloBridge, allowing community users to suggest additions to the public ontology. Complete the template below to submit a term request directly to the ontology maintainer.

Term Label (required)
Suggested term name. If a term can be described with multiple synonyms, only list the preferred name here.
Example: tissue-based format

Term description (required)
A brief definition, description, or usage of your suggested term. Additional term synonyms may be listed in this section.
Example: Involves the use of a tissue derived from a living organism and is a heterogeneous assay type.

Superclass (required)
The parent term of the suggested term. The parent term should be an existing entry of the current ontology. The superclass can be selected directly from the 'Classes' viewer on Bioportal's left tree navigation.
Example: assay format

References (optional)
Provide evidence for the existence of the requested term such as PMIDs of papers or links to other resources that describe the term.

Justification (optional)
Provide any additional information about the requested term here.

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