PMO Precision Medicine Ontology

Last uploaded: December 16, 2020
Preferred Name

Arthrogryposis

Synonyms
ID

http://www.phoc.org.cn/pmo/class/PMO_00037703

Database_Cross_Reference

HPO:HP:0002804

MEDCIN:32602

CHV:0000001476

SNOMEDCT_US:205402004

MTH:NOCODE

LCH:U000373

SNOMEDCT_US:77016009

SNOMEDCT_US:111246005

OMIM:MTHU003213

ICD10CM:Q74.3

SNOMEDCT_US:205107002

SNMI:D4-00601

MEDCIN:96815

OMIM:MTHU033304

JABL:39

SNOMEDCT_US:203040006

RCD:PFy2.

RCD:X7886

MTHICD9:728.3

OMIM:MTHU023157

MDR:10051643

NCI:C84572

RCD:XE1Fi

CCPSS:0061737

ICD10AM:Q74.3

SNOMEDCT_US:205403009

MSH:D001176

SNMI:D1-502A0

SNM:M-31750

LCH_NW:sh85008129

NDFRT:N0000000483

OMIM:MTHU009867

SNM:M-22460

OMIM:MTHU029230

ICD10:Q74.3

NCI_NICHD:C84572

CSP:0726-3953

RCD:PFy0.

SNM:D-8036

RCD:PE8y5

OMIM:MTHU006125

label

Arthrogryposis

MCID

MC00001269

PMOID

PMO:00037703

prefixIRI

pmo:PMO_00037703

prefLabel

Arthrogryposis

Synonym

Arthrogryposis (disorder)

Myodystrophia fetalis deformans

Myophagism congenita

Guerin Stern syndrome

AMC - Arthrogryp multi congeni

Syndrome, Guerin-Stern

multiple congenital contractures

Multiplex Congenitas, Arthrogryposis

Arthrogryposis Multiplex Congenitas (AMC)

Syndrome, Guérin-Stern

Arthrogryposis, congenital

Multiplex Congenitas, Arthrogryposis (AMC)

Arthrogryposis multiplex congenita

Otto Syndrome

Arthrogryposis (& [multiplex congenita]) (disorder)

arthrogryposis multiplex congenita

Congenital multiplex arthrogryposis

Arthromyodysplasia, Congenital

arthrogryposis (diagnosis)

Rossi's syndrome

Rocher Sheldon Syndrome

Guérin Stern Syndrome

Arthrogryp multiplex congenita

congenital arthromyodysplastic syndrome

Arthrogryposis, unspecified

Congenital Multiple Arthrogryposes

congenital contractures of extremities

Arthrogryposis Multiplex Congenita

Congenital Arthromyodysplasias

arthrogryposis multiplex congenita (diagnosis)

Rossi Syndrome

AMYOPLASIA CONGEN

Amyoplasia Congenita

Arthrogryposis, unspecified (disorder)

amyoplasia congenita

Congenita, Arthrogryposis Multiplex (AMC)

Arthrogryposis (& [multiplex congenita])

myodystrophia foetalis deformans

Myodystrophia foetalis deformans

myodysplasia fibrosa multiplex

Guérin-Stern Syndrome

Amyoplasia congenita

Classic arthrogryposis

Multiplex Congenita, Arthrogryposis

Otto syndrome

Syndrome, Rossi

AMC - Arthrogryposis multiplex congenita

Multiple Arthrogryposes, Congenital

Rocher-Sheldon syndrome

Multiple Arthrogryposis, Congenital

Myodystrophia Fetalis Deformans

Guerin Stern Syndrome

Arthrogryposis multiplex

ARTHROGRYPOSIS

Congenitas, Arthrogryposis Multiplex (AMC)

myodysplasia foetalis deformans

Rossi syndrome

Arthrogryposes

arthrogryposis multiplex congenita (AMC)

arthrogryposes

Syndrome, Otto

Arthromyodysplasias, Congenital

myodystrophia fetalis deformans

Guerin-Stern syndrome (disorder)

Arthrogryposis, Congenital Multiple

Arthrogryposis Multiplex Congenitas

Congenital contractures, multiple

Arthrogryposis multiplex congenita.

CONGEN ARTHROMYODYSPLASIA

neuro-arthromyodysplasia

Arthrogryposis multiplex congenita (disorder)

Guerin-Stern Syndrome

Arthrogryposis [Disease/Finding]

multiple congenital contracture

Guerin-Stern syndrome

Congenitas, Arthrogryposis Multiplex

Congenital Multiple Arthrogryposis

Syndrome, Rocher-Sheldon

Congenital Arthromyodysplasia

arthrogryposis

Arthrogryposes, Congenital Multiple

Arthrogryposis Multiplex Congenita (AMC)

Multiplex Congenita, Arthrogryposis (AMC)

ARTHROMYODYSPLASIA CONGEN

Congenital arthromyodysplasia

syndrome otto

Congenita, Arthrogryposis Multiplex

Fibrous Ankylosis of Multiple Joints

Multiple congenital contractures

Rocher-Sheldon Syndrome

Congenital multiple arthrogryposis

Tree Number

T9.8.3.7.14

T9.3.6.14

T9.3.10.26

T9.21.13.1.26

T9.3.1.26

subClassOf

http://www.phoc.org.cn/pmo/class/PMO_00001312

http://www.phoc.org.cn/pmo/class/PMO_00037723

http://www.phoc.org.cn/pmo/class/PMO_00013906

http://www.phoc.org.cn/pmo/class/PMO_00009573

http://www.phoc.org.cn/pmo/class/PMO_00039938

http://www.phoc.org.cn/pmo/class/PMO_00037691

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Delete Mapping To Ontology Source
http://www.ebi.ac.uk/efo/EFO_0003857 EFO LOOM
http://purl.obolibrary.org/obo/MONDO_0008779 MONDO LOOM
http://www.limics.org/hrdo/rdfns#sgn_id_18800 HRDO LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.660.077 RH-MESH LOOM
http://purl.bioontology.org/ontology/RCD/XE1Fi RCD LOOM
http://purl.obolibrary.org/obo/NCIT_C84572 BERO LOOM
http://purl.jp/bio/4/id/200906081055806116 IOBC LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#Arthrogryposis CSEO LOOM
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C84572 NCIT LOOM
http://purl.bioontology.org/ontology/OMIM/MTHU033304 OMIM LOOM
http://purl.bioontology.org/ontology/MESH/D001176 MESH LOOM
http://purl.bioontology.org/ontology/SNOMEDCT/111246005 SNOMEDCT LOOM
http://id.nlm.nih.gov/mesh/D001176 MDM LOOM
http://purl.bioontology.org/ontology/HL7/C0003886 HL7 LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C16.131.621.077 RH-MESH LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#1476 OCHV LOOM
http://purl.bioontology.org/ontology/LNC/LA29642-8 LOINC LOOM
http://purl.obolibrary.org/obo/MONDO_0008779 DOVES LOOM
http://purl.obolibrary.org/obo/OMIT_0002562 OMIT LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#D001176 RH-MESH LOOM
http://sbmi.uth.tmc.edu/ontology/ochv#C0003886 OCHV LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.651.102 RH-MESH LOOM
http://purl.bioontology.org/ontology/SNMI/D1-502A0 SNMI LOOM
http://purl.bioontology.org/ontology/RCTV2/N233000 RCTV2 LOOM
http://www.owl-ontologies.com/Ontology1358660052.owl#Arthrogryposis PEDTERM LOOM
http://www.gamuts.net/entity#arthrogryposis GAMUTS LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C05.550.150 RH-MESH LOOM