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Arthrogryposis multiplex congenita, CHRNB1-related, cattle
MONDO:1012772Any arthrogryposis multiplex congenita that occurs in cattle due to a mutation in the CHRNB1 gene.
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Disease
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Arthrogryposis multiplex congenita, cattle
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Arthrogryposis multiplex congenita, non-human animal
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Developmental defect during embryogenesis, non-human animal
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Disorder of development or morphogenesis, non-human animal
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Hereditary disease, non-human animal
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Non-human animal disease
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