Preferred Name

Down Syndrome

Synonyms
Definitions

A chromosomal dysgenesis syndrome resulting from a triplication or translocation of chromosome 21. Down syndrome occurs in approximately 1:700 live births. Abnormalities are variable from individual to individual and may include mental retardation, retarded growth, flat hypoplastic face with short nose, prominent epicanthic skin folds, small low-set ears with prominent antihelix, fissured and thickened tongue, laxness of joint ligaments, pelvic dysplasia, broad hands and feet, stubby fingers, transverse palmar crease, lenticular opacities and heart disease. Patients with Down syndrome have an estimated 10 to 30-fold increased risk for leukemia; most have symptoms of Alzheimer's disease by age 40. Also known as trisomy 21 syndrome.

ID

http://purl.obolibrary.org/obo/NCIT_C2993

ALT_DEFINITION

A disorder caused by the presence of an extra chromosome 21 and characterized by mental retardation and distinguishing physical features.

A chromosomal dysgenesis syndrome resulting from a triplication or translocation of chromosome 21. This condition is characterized by distinctive facial and physical features: short stature, developmental delay, cardiac defects (atrioventricular septal defect, tetralogy of Fallot), hypo- and hyperthyroidism, autoimmune disease (type 1 diabetes mellitus), and hypogonadism.

code

C2993

Contributing_Source

Cellosaurus

CPTAC

NICHD

PCDC

definition

A chromosomal dysgenesis syndrome resulting from a triplication or translocation of chromosome 21. Down syndrome occurs in approximately 1:700 live births. Abnormalities are variable from individual to individual and may include mental retardation, retarded growth, flat hypoplastic face with short nose, prominent epicanthic skin folds, small low-set ears with prominent antihelix, fissured and thickened tongue, laxness of joint ligaments, pelvic dysplasia, broad hands and feet, stubby fingers, transverse palmar crease, lenticular opacities and heart disease. Patients with Down syndrome have an estimated 10 to 30-fold increased risk for leukemia; most have symptoms of Alzheimer's disease by age 40. Also known as trisomy 21 syndrome.

in_subset

http://purl.obolibrary.org/obo/NCIT_C90259

http://purl.obolibrary.org/obo/NCIT_C158520

http://purl.obolibrary.org/obo/NCIT_C186341

http://purl.obolibrary.org/obo/NCIT_C156952

http://purl.obolibrary.org/obo/NCIT_C158035

http://purl.obolibrary.org/obo/NCIT_C165258

http://purl.obolibrary.org/obo/NCIT_C186315

http://purl.obolibrary.org/obo/NCIT_C99147

label

Down Syndrome

Legacy Concept Name

Down_Syndrome

Preferred_Name

Down Syndrome

prefixIRI

NCIT:C2993

prefLabel

Down Syndrome

Semantic_Type

Disease or Syndrome

UMLS_CUI

C0013080

subClassOf

http://purl.obolibrary.org/obo/NCIT_C3101

http://purl.obolibrary.org/obo/NCIT_C28193

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Delete Mapping To Ontology Source
http://www.ebi.ac.uk/efo/EFO_0001064 EFO LOOM
http://purl.obolibrary.org/obo/DOID_14250 DOID LOOM
http://purl.obolibrary.org/obo/MONDO_0008608 MONDO LOOM
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 DOVES LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C2993 NCIT 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 BAO 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://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