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
1 clinical trial for this condition and its sub-types.
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Disease
(717)
Syndromic disease
(25)
Human disease
(15)
Developmental defect during embryogenesis
(8)
Multiple congenital anomalies/dysmorphic syndrome
(1)
Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
(1)
Disease by body system or component
(0)
Disease by developmental or physiological process
(0)
Disorder of development or morphogenesis
(0)