loading...| Preferred Name |
Arthrogryposis Multiplex Congenita |
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| Synonyms |
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| Definitions |
A non-progressive finding characterized by multiple joint contractures found throughout the body at birth. |
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| ID |
http://www.phoc.org.cn/pmo/class/PMO_00001313 |
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| 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 |
|
| Definition |
A non-progressive finding characterized by multiple joint contractures found throughout the body at birth. |
|
| equivalentClass | ||
| label |
Arthrogryposis Multiplex Congenita |
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| MCID |
MC00001269 |
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| PMOID |
PMO:00001313 |
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| prefixIRI |
pmo:PMO_00001313 |
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| prefLabel |
Arthrogryposis Multiplex Congenita |
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| Synonym |
Arthrogryposis (disorder) Myodystrophia fetalis deformans Myophagism congenita AMC - Arthrogryp multi congeni Syndrome, Guerin-Stern Multiplex Congenitas, Arthrogryposis Arthrogryposis Multiplex Congenitas (AMC) Syndrome, Guérin-Stern Arthrogryposis, congenital Multiplex Congenitas, Arthrogryposis (AMC) Arthrogryposis multiplex congenita Arthrogryposis (& [multiplex congenita]) (disorder) 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 Congenital Arthromyodysplasias arthrogryposis multiplex congenita (diagnosis) AMYOPLASIA CONGEN Arthrogryposis, unspecified (disorder) Congenita, Arthrogryposis Multiplex (AMC) Arthrogryposis (& [multiplex congenita]) 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 Guerin Stern Syndrome Arthrogryposis multiplex Congenitas, Arthrogryposis Multiplex (AMC) myodysplasia foetalis deformans Rossi syndrome Arthrogryposes arthrogryposis multiplex congenita (AMC) Syndrome, Otto Arthromyodysplasias, Congenital Guerin-Stern syndrome (disorder) Arthrogryposis, Congenital Multiple Arthrogryposis Multiplex Congenitas Congenital contractures, multiple Arthrogryposis multiplex congenita. CONGEN ARTHROMYODYSPLASIA neuro-arthromyodysplasia Arthrogryposis multiplex congenita (disorder) Arthrogryposis Arthrogryposis [Disease/Finding] multiple congenital contracture Guerin-Stern syndrome Congenitas, Arthrogryposis Multiplex Syndrome, Rocher-Sheldon Arthrogryposes, Congenital Multiple Multiplex Congenita, Arthrogryposis (AMC) ARTHROMYODYSPLASIA CONGEN Congenital arthromyodysplasia syndrome otto Congenita, Arthrogryposis Multiplex Fibrous Ankylosis of Multiple Joints Multiple congenital contractures Congenital multiple arthrogryposis |
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| Tree Number |
T3.1.5.7.2 |
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| 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 |