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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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Autosomal genetic disease
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Autosomal dominant disease
Distal arthrogryposis type 2B1
rare
Identifiers
MONDO:0020820
OMIM:601680
Causal genes
TNNI2
Part of
Sheldon-hall syndrome
Autosomal dominant disease
Also known as
arthrogryposis, distal, type 2B1 · DA2B1
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