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Fryns syndrome
MONDO:0009253Fryns syndrome (FS) is a multiple congenital anomaly syndrome characterized by dysmorphic facial features, congenital diaphragmatic hernia, pulmonary hypoplasia, and distal limb hypoplasia, in addition to variable expression of additional malformations.
Also known as: Fryns syndrome, diaphragmatic hernia-abnormal face-distal limb anomalies syndrome, FRNS, Moerman Van den Berghe Fryns syndrome, diaphragmatic hernia, abnormal face, and distal limb anomalies
5 clinical trials for this condition and its sub-types.
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Disease
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Syndromic disease
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Human disease
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Developmental defect during embryogenesis
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Multiple congenital anomalies/dysmorphic syndrome
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Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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Disease by body system or component
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Disease by developmental or physiological process
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Disorder of development or morphogenesis
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