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Braddock syndrome

Disease Summary
Associated Targets ()

Mondo Description Braddock syndrome is a rare malformation syndrome with multiple congenital abnormalities, described in 2 siblings, that is characterized by VACTERL -like association in combination with pulmonary hypertension, laryngeal webs, blue sclerae, abnormal ears, persistent growth deficiency and normal intellect.
Mondo Term and Equivalent IDs
MONDO:0012032:  Braddock syndrome
MESH:C564244: 
Orphanet:52047: 
SCTID:720575002: 
UMLS:C1842082: 
UMLS:C4303988: