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RGD uses the Human Disease Ontology (DO, for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

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Accession:DOID:9000338 term browser browse the term
This term is obsolete. We suggest searching for the text of the ontology term or for a keyword rather than searching for the ontology ID. For more information, please contact us.
Definition:Persistent flexure or contracture of a joint. 
Synonyms:exact_synonym: Arthrogryposis Multiplex Congenita (AMC);   Congenital Arthromyodysplasia;   Congenital Arthromyodysplasias;   Congenital Multiple Arthrogryposes;   Congenital Multiple Arthrogryposis;   Fibrous Ankylosis of Multiple Joints;   Guerin Stern Syndrome;   Guérin Stern Syndrome;   Myodystrophia Fetalis Deformans;   Otto syndrome;   Rocher Sheldon syndrome;   Rossi syndrome;   amyoplasia congenita;   arthrogryposes;   arthrogryposis multiplex congenita
 xref: NCI:C84572;   OMIM:PS617468
 replaced_by: DOID:0080954
For additional species annotation, visit the Alliance of Genome Resources.

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