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Disease association ontology term - MONDO:0015168 - arthrogryposis multiplex congenita

Term summary

ID
MONDO:0015168
Name
arthrogryposis multiplex congenita
Ontology or CV name
Disease association
Definition
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.

Parents

Annotation

Disease association

MONDO:0032903 - arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum

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MONDO:0030281 - arthrogryposis multiplex congenita 6

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MONDO:0975826 - arthrogryposis multiplex congenita 7, X-linked

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MONDO:0008822 - arthrogryposis, renal dysfunction, and cholestasis 1

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MONDO:0017123 - arthrogryposis-renal dysfunction-cholestasis syndrome

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MONDO:0100101 - fetal akinesia deformation sequence 1

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MONDO:0100104 - fetal akinesia deformation sequence 4

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MONDO:0010532 - infantile-onset X-linked spinal muscular atrophy

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MONDO:0012750 - lethal arthrogryposis-anterior horn cell disease syndrome

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MONDO:0014552 - lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome

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MONDO:0014806 - spinal muscular atrophy with congenital bone fractures 1

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MONDO:0014807 - spinal muscular atrophy with congenital bone fractures 2

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