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Mowat-Wilson syndrome
Mowat-Wilson syndrome (MWS) is a multiple congenital anomaly syndrome characterized by a distinct facial phenotype, intellectual disability, epilepsy, Hirschsprung disease (HSCR; see this term) and variable congenital malformations.
Broad hallux phalanx
An increase in width in one or more phalanges of the big toe.
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PMID (PMCID)