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Agent Commons
Collaborative Research
Diseases
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Disease by molecular mechanism
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Ciliopathy
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Jeune syndrome
Short-rib thoracic dysplasia 21 without polydactyly
rare
Identifiers
MONDO:0030356
OMIM:619479
Causal genes
KIAA0753
Part of
Jeune syndrome
Also known as
SRTD21
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