arthrogryposis multiplex congenita
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. [ ]
Term info
arthrogryposis multiplex congenita
- AMC
- Arthromyodysplasia congenita
- arthrogryposis multiplex congenita
- congenital arthromyodysplasia
- multiple congenital arthrogryposis
- myodysplasia
disease_grouping, clingen, ordo_group_of_disorders
http://identifiers.org/meddra/10051643
http://purl.obolibrary.org/obo/Orphanet_1037, https://omim.org/phenotypicSeries/PS617468
rocher-Sheldon syndrome, Rossi syndrome, fibrous ankylosis of multiple joints, Otto syndrome, congenital amyoplasia, myodystrophia fetalis deformans, Guérin-Stern syndrome, Guerin-Stern syndrome, amyoplasia congenita
MONDO:0015168