BioAssay Ontology

Last uploaded: February 21, 2024
Preferred Name

Down syndrome

Synonyms

trisomy 21 syndrome

Definitions

OMIM mapping confirmed by DO. [SN]. A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability.

ID

http://purl.obolibrary.org/obo/DOID_14250

comment

OMIM mapping confirmed by DO. [SN].

database_cross_reference

UMLS_CUI:C0013080

SNOMEDCT_US_2020_03_01:41040004

OMIM:190685

MESH:D004314

ICD10CM:Q90

ICD9CM:758.0

GARD:10247

NCI:C2993

ORDO:870

has exact synonym

trisomy 21 syndrome

G Trisomy

Down's syndrome

Complete trisomy 21 syndrome

Downs syndrome

Down's syndrome - trisomy 21

has_obo_namespace

disease_ontology

id

DOID:14250

imported from

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

in_subset

http://purl.oboInOwllibrary.org/oboInOwl/doid#NCIthesaurus

http://purl.oboInOwllibrary.org/oboInOwl/doid#DO_FlyBase_slim

label

Down syndrome

notation

DOID:14250

prefLabel

Down syndrome

textual definition

A chromosomal disease that is characterized by flat-looking facial features and weak muscle tone (hypotonia) in infancy and is caused by trisomy of all or a critical portion of chromosome 21 and is associated with intellectual disability.

subClassOf

http://purl.obolibrary.org/obo/DOID_0060429

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/DOID_14250 DTO SAME_URI
http://purl.obolibrary.org/obo/DOID_14250 DOID SAME_URI
http://purl.obolibrary.org/obo/DOID_14250 EPIO SAME_URI
http://purl.obolibrary.org/obo/DOID_14250 HHEAR SAME_URI
http://purl.obolibrary.org/obo/DOID_14250 NIFSTD SAME_URI
http://purl.obolibrary.org/obo/DOID_14250 FNS-H SAME_URI
http://purl.bioontology.org/ontology/ICD10CM/Q90 ICD10CM LOOM
http://www.owl-ontologies.com/unnamed.owl#RID14623 DERMLEX LOOM
http://localhost/plosthes.2017-1#5558 PLOSTHES LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0013080 OCHV LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.597.606.643.220 RH-MESH LOOM
http://www.co-ode.org/ontologies/galen#DownSyndrome GALEN LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.077.327 RH-MESH LOOM
http://cbmi.med.harvard.edu/asdphenotype#Class_181 ASDPTO LOOM
http://www.shojaee.com/shr/shr.owl#Down_Syndrome SHR LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.260.260 RH-MESH LOOM
http://www.owl-ontologies.com/Ontology1358660052.owl#Down_Syndrome PEDTERM LOOM
http://purl.obolibrary.org/obo/OGMD_0000065 OGMD LOOM
http://purl.bioontology.org/ontology/ICPC2P/A90001 ICPC2P LOOM
http://doe-generated-ontology.com/OntoAD#C0013080 ONTOAD LOOM
http://purl.bioontology.org/ontology/MESH/D004314 MESH LOOM
http://purl.obolibrary.org/obo/OMIT_0005570 OMIT LOOM
http://www.orpha.net/ORDO/Orphanet_870 ORDO LOOM
http://purl.obolibrary.org/obo/MONDO_0008608 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0008608 DOVES LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2993 NCIT LOOM
http://www.ebi.ac.uk/efo/EFO_0001064 EFO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.180.260 RH-MESH LOOM
http://purl.obolibrary.org/obo/DOID_14250 DTO LOOM
http://purl.obolibrary.org/obo/DOID_14250 DOID LOOM
http://purl.obolibrary.org/obo/DOID_14250 EPIO LOOM
http://purl.obolibrary.org/obo/DOID_14250 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_14250 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_14250 FNS-H LOOM
http://purl.obolibrary.org/obo/NCIT_C2993 BERO LOOM
http://www.projecthalo.com/aura#Down-Syndrome AURA LOOM
http://www.phoc.org.cn/pmo/class/PMO_00040029 PMAPP-PMO LOOM
http://www.limics.org/hrdo/rdfns#pat_id_116 HRDO LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#4101 OCHV LOOM
http://neuromorpho.org/ontologies/experimentconditionH.owl#NMOOt_244 NMOBR LOOM
http://purl.bioontology.org/ontology/OMIM/190685 OMIM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D004314 RH-MESH LOOM
http://purl.jp/bio/4/id/200906084461038234 IOBC LOOM
http://purl.obolibrary.org/obo/GSSO_001812 GSSO LOOM
http://www.semanticweb.org/mypc/ontologies/2022/11/USBirthOnto-22#DownSyndrome BIRTHONTO LOOM
http://purl.bioontology.org/ontology/LNC/LA20088-3 LOINC LOOM

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.

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Example: Involves the use of a tissue derived from a living organism and is a heterogeneous assay type.

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