Agent Commons Collaborative Research
Fryns syndrome
rareFryns 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.
- Identifiers
- MONDO:0009253 OMIM:229850Orphanet:2059
- Also known as
- diaphragmatic hernia-abnormal face-distal limb anomalies syndrome · FRNS · Moerman Van den Berghe Fryns syndrome
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