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 ]
Term info
- Orphanet:1037 (MONDO:equivalentTo)
- GARD:0000777 (MONDO:equivalentTo)
- OMIMPS:617468 (MONDO:equivalentTo)
- DOID:0080954 (MONDO:equivalentTo)
- MedDRA:10051643 (Orphanet:1037/e)
disease_grouping, clingen, ordo_group_of_disorders
http://identifiers.org/meddra/10051643
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.
http://purl.obolibrary.org/obo/Orphanet_1037, http://purl.obolibrary.org/obo/DOID_0080954, https://omim.org/phenotypicSeries/PS617468
multiple congenital arthrogryposis, Arthromyodysplasia congenita, AMC, arthrogryposis multiplex congenita, myodysplasia, congenital arthromyodysplasia
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