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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
/
Hereditary disease
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Distal arthrogryposis
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Digitotalar dysmorphism
Arthrogryposis, distal, type 1B
rare
Identifiers
MONDO:0013698
OMIM:614335
Causal genes
MYBPC1
Part of
Digitotalar dysmorphism
Also known as
DA1B
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