FB2025_05 , released December 11, 2025

CV Term Report

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General Information
Term	arthrogryposis multiplex congenita	ID (Ontology)	DOID:0080954 (Human Disease)
Definition	A nervous system disease that is characterized by development of multiple joint contractures affecting two or more areas of the body prior to birth.
Comment
Links to External Ontologies
	DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
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Spanning Tree (Parents/Children)

autosomal genetic disease
 |__autosomal recessive disease__
disease                          |
 |__physical disorder____________|
disease of anatomical entity     |
 |__nervous system disease_______|
                                 arthrogryposis multiplex congenita  5 rec.
                                  |__arthrogryposis multiplex congenita-1
                                  |__arthrogryposis multiplex congenita-3 1 rec.
                                  |__arthrogryposis multiplex congenita-4 2 rec.
                                  |__arthrogryposis multiplex congenita-5 1 rec.
                                  |__arthrogryposis multiplex congenita-6
                                  |__neurogenic-type arthrogryposis multiplex congenita-2 1 rec.

Spanning Tree View Settings
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Relationships
Is a	autosomal recessive disease physical disorder nervous system disease
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Synonyms & Secondary IDs
Synonyms

Secondary IDs

External Crossreferences & Linkouts
	GARD:777 MIM:PS617468