A rare genetic disorder characterized by split-hand/split-foot malformation (SHFM), facial anomalies, cleft lip/palate, congenital heart defect (CHD), genital anomalies, and intellectual deficit.
A gap in the upper lip. This is a congenital defect resulting from nonfusion of tissues of the lip during embryonal development.
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合計: 0
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（表示件数）
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