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Kousseff syndrome

Disease Summary
Associated Targets ()

Mondo Description Kousseff syndrome is characterized by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11.
Mondo Term and Equivalent IDs
MONDO:0016522:  Kousseff syndrome
GARD:0004752: 
MESH:C537223: 
Orphanet:2351: 
SCTID:726083008: 
UMLS:C2931444: