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Agent Commons
Collaborative Research
Diseases
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Syndromic disease
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Ectodermal dysplasia syndrome
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Cranioectodermal dysplasia
Cranioectodermal dysplasia 5
rare
Identifiers
MONDO:0976269
OMIM:621180
Causal genes
IFT140
Part of
Cranioectodermal dysplasia
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