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Okamoto syndrome

Disease Summary
Associated Targets ()

Mondo Description Okamoto syndrome is characterised by congenital hydronephrosis, intellectual deficit, growth retardation, cleft palate, generalised hypotonia and a characteristic face. Cardiac anomalies have also been reported. To date, 6 cases have been reported.
Mondo Term and Equivalent IDs
MONDO:0011499:  Okamoto syndrome
GARD:0004064: 
MESH:C565736: 
Orphanet:2729: 
SCTID:722065002: 
UMLS:C1858043: