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Fryns syndrome

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description Fryns 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.
Mondo Term and Equivalent IDs
MONDO:0009253:  Fryns syndrome
GARD:0003699: 
MESH:C538070: 
NCIT:C98932: 
Orphanet:2059: 
SCTID:702432006: 
UMLS:C0220730: