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 myodysplasia arthrogryposis multiplex congenita congenital arthromyodysplasia
Term information
- MEDGEN:1830310 (MONDO:equivalentTo)
- NORD:810 (MONDO:NORD)
- MedDRA:10051643 (Orphanet:1037/e)
- UMLS:C5779613 (MONDO:equivalentTo)
- DOID:0080954 (MONDO:equivalentTo)
- OMIMPS:617468 (MONDO:equivalentTo)
- icd11.foundation:1930990330 (Orphanet:1037)
- Orphanet:1037 (MONDO:equivalentTo)
- GARD:777 (MONDO:GARD)
gard_rare, matrix_llm__is_cancer_other, matrix_llm__is_glucose_dysfunction_other, otar, matrix_llm__tag_qualy_lost_other, disease_grouping, harrisons_view_disorder_of_development_or_morphogenesis, matrix_llm__medical_specialization_other, matrix_llm__txgnn_other, mondo_top_grouping_member, mondo_top_grouping_hereditary_disease, matrix_included, matrix_llm__tag_existing_treatment_other, nord_rare, clingen, matrix_txgnn_grouping_other, matrix_llm__anatomical_other, matrix_llm__is_pathogen_caused_other, rare, harrisons_view_member, harrisons_view_hereditary_disease, mondo_top_grouping_disorder_of_development_or_morphogenesis, ordo_group_of_disorders
http://identifiers.org/medgen/1830310
http://purl.obolibrary.org/obo/mondo/sources/icd11foundation/1930990330
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
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