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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Arthrogryposis multiplex congenita
Arthrogryposis multiplex congenita 5
rare
Identifiers
MONDO:0100218
OMIM:618947
Causal genes
TOR1A
Part of
Arthrogryposis multiplex congenita
Also known as
AMC5
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