PMO Precision Medicine Ontology

Last uploaded: December 16, 2020
Preferred Name

Turner Syndrome
Synonyms
ID

http://www.phoc.org.cn/pmo/class/PMO_00036238

Database_Cross_Reference

ICPC2P:A90009

MTHICD9:758.6

CCPSS:1013623

PSY:54460

ICD10CM:Q96.9

MTH:NOCODE

ICD10CM:Q96.0

MEDLINEPLUS:3684

ICD10AM:Q96.9

ICD10:Q96.0

DXP:U004172

ICD10:Q96.9

MDR:10048226

ICD10:Q96

RCD:PJ631

COSTAR:NOCODE

NCI:C26900

SNMI:D4-00302

LCH_NW:sh85138930

JABL:220

LCH:U004825

SNM:D-5743

MEDCIN:331214

NDFRT:N0000003057

SNOMEDCT_US:38804009

ICD10AM:Q96.0

CHV:0000012667

MSH:D014424

SNOMEDCT_US:268299006

NCI:C85210

CSP:1254-8447

DO:DOID:3491

SNOMEDCT_US:268356004

SNOMEDCT_US:205691005

SNOMEDCT_US:157020008

SNMI:D4-02272

RCD:PJ63.

MEDLINEPLUS:1504

SNM:D-5028

ICD10CM:Q96

SNOMEDCT_US:205685008

DXP:NOCODE

NCI_NICHD:C26900

MEDCIN:30425

SNM:D-2667

RCD:XE1Mf

MDR:10045181

ICD10AM:Q96

label

Turner Syndrome

MCID

MC00013239

PMOID

PMO:00036238

prefixIRI

pmo:PMO_00036238

prefLabel

Turner Syndrome

Synonym

DWARFISM, OVARIAN

Ullrich Turner Syndrome

Gonadal Dysgenesis

Morgagni-Turner syndrome

Turner syndrome (diagnosis)

Turner syndrome

turner syndrome

Syndrome, Ullrich-Turner

Morgagni-Turner-Albright syndrome

Turner syndrome (TS)

Turner syndrome (disorder)

gonadal dysgenesis

Turner Syndrome [Disease/Finding]

turner's syndrome

XO syndrome

gonadal dysgenesis syndrome

45X0 - Turner's syndrome

Pterygolymphangiectasia syndrome

Turners Syndrome

TS - Turner's syndrome

pseudonuchal infantilism

X0 - Turner's syndrome

Turner's syndrome, unspecified

Karyotype 45, X

ovarian short stature syndrome

TURNER-VARNY SYNDROME

genital dwarfism

XO genotype

Turner's syndrome

bonnevie-ullrich syndrome

XO SYNDROME

Karyotype 45,X

ovarian dwarfism

Turner Syndrome (XO Syndrome)

primary ovarian insufficiency

Turner's Syndrome

Bonnevie-Ullrich syndrome

Ullrich-Turner syndrome (UTS)

45, X syndrome

ULLRICH-TURNER SYNDROME

Gonadal dysgenesis - Turner

xo syndrome

Monosomy X

Turner syndrome karyotype 45,X (diagnosis)

chromosome XO syndrome

Karyotype 45, X (disorder)

Ullrich-Turner syndrome

Shereshevskii-Turner syndrome

TURNER SYNDROME

Turner syndrome karyotype 45, X

XO Syndrome

Turner's syndrome NOS

Primary ovarian insufficiency

Ullrich-Turner Syndrome

monosomy X syndrome

Turner syndrome karyotype 45,X

Turner-Albright syndrome

Turner's syndrome NOS (disorder)

Turner syndrome, NOS

Tree Number

T9.20.3.1.10

T9.9.9.5.4.2

T9.9.9.5.6.2

T9.24.4.6.6.2

T9.20.1.3.10

T9.19.2.5.6.6.2

T9.8.4.32.15.1.2

T9.24.4.6.4.2

T9.8.3.11.6.4.2

T9.19.2.5.6.4.2

T9.8.3.11.6.6.2

T9.8.3.9.15.1.2

T9.8.3.3.1.10

subClassOf

http://www.phoc.org.cn/pmo/class/PMO_00004451

http://www.phoc.org.cn/pmo/class/PMO_00040060

http://www.phoc.org.cn/pmo/class/PMO_00036216

http://www.phoc.org.cn/pmo/class/PMO_00037261

Delete Subject Author Type Created
No notes to display
Create mapping

Delete Mapping To Ontology Source
http://purl.bioontology.org/ontology/SNOMEDCT/38804009 SNOMEDCT LOOM
http://www.orpha.net/ORDO/Orphanet_881 ORDO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C14.280.400.980 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C19.391.119.795.750 RH-MESH LOOM
http://localhost/plosthes.2017-1#350 PLOSTHES LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.939.316.309.872 RH-MESH LOOM
rgo:29526 GAMUTS LOOM
http://purl.obolibrary.org/obo/OMIT_0015260 OMIT LOOM
http://www.projecthalo.com/aura#Turner-Syndrome AURA LOOM
http://purl.obolibrary.org/obo/MONDO_0019499 CCONT LOOM
http://purl.obolibrary.org/obo/MONDO_0019499 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0019499 MONDO LOOM
http://purl.obolibrary.org/obo/MONDO_0019499 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0019499 DOVES LOOM
http://purl.obolibrary.org/obo/MONDO_0019499 KTAO LOOM
http://purl.obolibrary.org/obo/DOID_3491 DTO LOOM
http://purl.obolibrary.org/obo/DOID_3491 DOID LOOM
http://purl.obolibrary.org/obo/DOID_3491 BAO LOOM
http://purl.obolibrary.org/obo/DOID_3491 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_3491 DDSS LOOM
http://purl.obolibrary.org/obo/DOID_3491 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_3491 MIDO LOOM
http://purl.obolibrary.org/obo/DOID_3491 FNS-H LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C26900 NCIT LOOM
http://www.owl-ontologies.com/Ontology1358660052.owl#Turner_Syndrome PEDTERM LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.939.316.795.750 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D014424 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C13.351.875.253.309.872 RH-MESH LOOM
http://www.limics.org/hrdo/rdfns#pat_id_44 HRDO LOOM
http://purl.bioontology.org/ontology/MESH/D014424 MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C14.240.400.980 RH-MESH LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Turner_s_Syndrome CSEO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.180.830.835.750 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.240.400.970 RH-MESH LOOM
http://vocab.vodan-totafrica.info/vodana-terms/vdiseases/LD50.0 VODANADISEASES LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C13.351.875.253.795.750 RH-MESH LOOM
http://nanbyodata.jp/ontology/NANDO_2200410 NANDO LOOM
http://purl.obolibrary.org/obo/NCIT_C26900 BERO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C12.706.316.795.750 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.260.830.835.750 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C12.706.316.309.872 RH-MESH LOOM
http://purl.bioontology.org/ontology/ICPC2P/A90009 ICPC2P LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C19.391.119.309.872 RH-MESH LOOM
http://purl.obolibrary.org/obo/OGMD_0000073 OGMD LOOM
http://www.co-ode.org/ontologies/galen#TurnerSyndrome GALEN LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0041408 MEDLINEPLUS LOOM
http://www.owl-ontologies.com/unnamed.owl#RID14628 DERMLEX LOOM