PMO Precision Medicine Ontology

Last uploaded: December 16, 2020
Preferred Name

Prader-Willi Syndrome

Synonyms
Definitions

A chromosomal disease that is characterized by weak muscle tone, feeding difficulties, poor growth, and delayed development. Beginning in childhood, affected individuals develop an insatiable appetite, which leads to chronic overeating and obesity.

ID

http://www.phoc.org.cn/pmo/class/PMO_00040030

Database_Cross_Reference

SNOMEDCT_US:205794007

NCI:C75463

MTH:NOCODE

SNOMEDCT_US:89392001

LCH_NW:sh85106050

DO:DOID:11983

SNMI:D4-00615

MDR:10036476

CHV:0000010026

CSP:1849-7731

ICD10CM:Q87.1

NCI_NICHD:C75463

ICD9CM:759.81

LCH:U003796

RCD:PKy93

DXP:U001571

SNM:D-5089

JABL:537

MSH:D011218

DXP:NOCODE

CCPSS:0023549

PSY:39867

OMIM:176270

MEDCIN:30417

NDFRT:N0000002472

MEDLINEPLUS:1243

Definition

A chromosomal disease that is characterized by weak muscle tone, feeding difficulties, poor growth, and delayed development. Beginning in childhood, affected individuals develop an insatiable appetite, which leads to chronic overeating and obesity.

label

Prader-Willi Syndrome

MCID

MC00010549

PMOID

PMO:00040030

prefixIRI

pmo:PMO_00040030

prefLabel

Prader-Willi Syndrome

Synonym

prader willy syndrome

Labhart-Willi Syndrome

PRADER-WILLI SYNDROME

prader willis syndrome

Prader-Willi syndrome

Syndrome, Labhart-Willi-Prader-Fanconi

Labhart Willi Syndrome

prader willi syndromes

cardiorespiratory syndrome of obesity in child

Labhart-Willi-Prader-Fanconi Syndrome

hypotonia-hypopigmentia-hypogonadism-obesity (HHHO) syndrome

Prader-Labhart-Willi syndrome

prader willies syndrome

Prader-Willi Syndrome [Disease/Finding]

H2O syndrome

Willi Prader Syndrome

Prader-Willi syndrome (PWS)

Syndrome, Prader-Labhart-Willi

prader syndrome willis

hypogenital dystrophy with diabetic tendency syndrome

Prader-Labhart-Willi (PLW) syndrome (PLWS)

Syndrome, Labhart-Willi

Prader Willi syndrome

Prader-Labhart-Willi-Fanconi syndrome

Labhart Willi Prader Fanconi Syndrome

hypotonia-obesity-hypogonadism-mental retardation syndrome

hypotonia-hypogonadism-obesity syndrome

hypotonia-hypopigmentia-hypogonadism-obesity syndrome

prader-willi syndrome

Prader Willi Syndrome

Willi-Prader Syndrome

PWS

prader syndrome willi

Syndrome, Willi-Prader

Prader-Willi syndrome (diagnosis)

willi prader syndrome

PRADER-LABHART-WILLI SYNDROME

PRADER WILLI SYNDROME

Syndrome, Prader-Willi

Prader-Labhart-Willi Syndrome

OBESITY-CRYPTORCHIDISM-DWARFISM-SUBNORMAL MENTALITY SYNDROME

syndrome willi prader

prader syndrome willies

Prader - Willi syndrome

prader willi syndrome

Prader Labhart Willi Syndrome

Prader-willi syndrome

Prader-Willi syndrome (disorder)

prader syndrome willy

syndrome prader-willi

Tree Number

T9.8.3.9.18

T3.25.90.5

T9.8.4.32.18

T9.11.2.1.1.3

T9.21.1.5.9.5

T3.25.70.9.5

T3.25.11.5.9.5

T9.8.3.1.56

subClassOf

http://www.phoc.org.cn/pmo/class/PMO_00085653

http://www.phoc.org.cn/pmo/class/PMO_00040090

http://www.phoc.org.cn/pmo/class/PMO_00040104

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Delete Mapping To Ontology Source
http://purl.obolibrary.org/obo/MONDO_0008300 MONDO LOOM
http://purl.obolibrary.org/obo/MESH_D011218 BERO LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/89392001 SNOMEDCT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.260.700 RH-MESH LOOM
http://purl.bioontology.org/ontology/SNMI/D4-00615 SNMI LOOM
http://purl.bioontology.org/ontology/OMIM/176270 OMIM LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#10026 OCHV LOOM
http://www.limics.org/hrdo/rdfns#pat_id_139 HRDO LOOM
http://purl.jp/bio/4/id/200906011442457180 IOBC LOOM
http://localhost/plosthes.2017-1#7162 PLOSTHES LOOM
http://purl.bioontology.org/ontology/CSP/1849-7731 CRISP LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.077.730 RH-MESH LOOM
http://nanbyodata.jp/ontology/NANDO_1200678 NANDO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.320.180.700 RH-MESH LOOM
http://purl.obolibrary.org/obo/OMIT_0012182 OMIT LOOM
http://www.projecthalo.com/aura#Prader-Willi-Syndrome AURA LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0032897 OCHV LOOM
http://www.owl-ontologies.com/NPOntology.owl#DOID_11983 NATPRO LOOM
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0032897 MEDLINEPLUS LOOM
http://purl.bioontology.org/ontology/RCD/PKy93 RCD LOOM
http://purl.obolibrary.org/obo/MONDO_0008300 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0008300 DOVES LOOM
http://purl.obolibrary.org/obo/Prader-Willi_Syndrome NND_ND LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Prader_Willi_Syndrome CSEO LOOM
http://cbmi.med.harvard.edu/asdphenotype#Class_500 ASDPTO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D011218 RH-MESH LOOM
http://www.gamuts.net/entity#Prader_Willi_syndrome GAMUTS LOOM
http://www.orpha.net/ORDO/Orphanet_739 ORDO LOOM
http://purl.bioontology.org/ontology/MESH/D011218 MESH LOOM
http://nanbyodata.jp/ontology/NANDO_2200411 NANDO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C18.654.726.500.740 RH-MESH LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C10.597.606.643.690 RH-MESH LOOM
http://purl.bioontology.org/ontology/ICD9CM/759.81 ICD9CM LOOM
http://purl.bioontology.org/ontology/ICD9CM/759.81 NLMVS LOOM
http://purl.obolibrary.org/obo/NCIT_C75463 BERO LOOM
http://ontology.apa.org/apaonto/termsonlyOUT%20(5).owl#Prader_Willi_Syndrome APADISORDERS LOOM
http://ontology.apa.org/apaonto/termsonlyOUT%20(5).owl#Prader_Willi_Syndrome APAONTO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C75463 NCIT LOOM
http://purl.bioontology.org/ontology/ICD10CM/Q87.11 ICD10CM LOOM
http://purl.obolibrary.org/obo/OGMD_0000072 OGMD LOOM
http://purl.obolibrary.org/obo/DOID_11983 CLO LOOM
http://purl.obolibrary.org/obo/DOID_11983 DTO LOOM
http://purl.obolibrary.org/obo/DOID_11983 DOID LOOM
http://purl.obolibrary.org/obo/DOID_11983 BAO LOOM
http://purl.obolibrary.org/obo/DOID_11983 HHEAR LOOM
http://purl.obolibrary.org/obo/DOID_11983 NIFSTD LOOM
http://purl.obolibrary.org/obo/DOID_11983 FNS-H LOOM
http://purl.bioontology.org/ontology/MEDDRA/10036476 MEDDRA LOOM
http://www.owl-ontologies.com/unnamed.owl#RID15350 DERMLEX LOOM
http://www.owl-ontologies.com/Ontology1358660052.owl#Prader-Willi_Syndrome PEDTERM LOOM
http://purl.bioontology.org/ontology/RCTV2/PKy9300 RCTV2 LOOM