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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.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
GARD:0004752
MESH:C537223
Orphanet:2351
SCTID:726083008
UMLS:C2931444
MONDO:0016522
High level summary of knowledge for a disease, including descriptions and datasource references.