arthrogryposis multiplex congenita

arthrogryposis multiplex congenita

http://purl.obolibrary.org/obo/MONDO_0015168

Arthrogryposis multiplex congenita (AMC) is a group of disorders characterized by congenital limb contractures. It manifests as limitation of movement of multiple limb joints at birth that is usually non-progressive and may include muscle weakness and fibrosis. AMC is always associated with decreased intrauterine fetal movement which leads secondarily to the contractures. [ Orphanet:1037 ]

Synonyms: multiple congenital arthrogryposis Arthromyodysplasia congenita AMC arthrogryposis multiplex congenita myodysplasia congenital arthromyodysplasia

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Term mappings

This is just here as a test because I lose it

Term information

database cross reference

icd11.foundation:1930990330 (Orphanet:1037)
OMIMPS:617468 (MONDO:equivalentTo)
MedDRA:10051643 (Orphanet:1037/e)
UMLS:C5779613 (MONDO:equivalentTo)
NORD:810 (MONDO:NORD)
MEDGEN:1830310 (MONDO:equivalentTo)
GARD:777 (MONDO:GARD)
DOID:0080954 (MONDO:equivalentTo)
Orphanet:1037 (MONDO:equivalentTo)

Subsets

gard_rare, otar, disease_grouping, rare, nord_rare, clingen, ordo_group_of_disorders

closeMatch

http://identifiers.org/meddra/10051643

exactMatch

http://identifiers.org/medgen/1830310

http://purl.obolibrary.org/obo/DOID_0080954

https://omim.org/phenotypicSeries/PS617468

http://linkedlifedata.com/resource/umls/id/C5779613

http://www.orpha.net/ORDO/Orphanet_1037

has related synonym

rocher-Sheldon syndrome

Rossi syndrome

fibrous ankylosis of multiple joints

Otto syndrome

congenital amyoplasia

Guérin-Stern syndrome

myodystrophia fetalis deformans

Guerin-Stern syndrome

amyoplasia congenita

MONDO:0015168

Term relations

Subclass of: