hereditary disease arthrogryposis multiplex congenita https://github.com/monarch-initiative/mondo/issues/9097 https://www.malacards.org/card/distal_arthrogryposis OMIMPS:617468 myodystrophia fetalis deformans icd11.foundation:1930990330 Rossi syndrome ICD10CM:Q74.3 GARD:0000777 fibrous ankylosis of multiple joints congenital arthromyodysplasia NORD:810 Guerin-Stern syndrome multiple congenital arthrogryposis MedDRA:10051643 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. MEDGEN:1830310 AMC Otto syndrome rocher-Sheldon syndrome myodysplasia Arthromyodysplasia congenita Orphanet:1037 Guérin-Stern syndrome UMLS:C5779613 arthrogryposis multiplex congenita DOID:0080954 arthrogryposis syndrome