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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
Arthrogryposis, distal, type 2B3
rare
Identifiers
MONDO:0032751
OMIM:618436
Causal genes
MYH3
Part of
Sheldon-hall syndrome
Autosomal dominant disease
Also known as
arthrogryposis, distal, type 2B3 (Sheldon-Hall) · DA2B3
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