You are using an outdated browser. Please upgrade your browser to improve your experience.

ulnar hypoplasia-split foot syndrome

Disease Summary
Associated Targets ()

Mondo Description Ulnar hypoplasia-split foot syndrome is characterised by the association of severe ulnar hypoplasia, absence of fingers two to five, and split-foot. It has been described in four males belonging to two generations of the same family. X-linked recessive inheritance is suggested, but autosomal dominant transmission cannot be excluded.
Mondo Term and Equivalent IDs
MONDO:0010750:  ulnar hypoplasia-split foot syndrome
GARD:0005400: 
MESH:C536936: 
Orphanet:1122: 
UMLS:C1839123: