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- Q55786282 description "Kousseff syndrome is characterized by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11 (see this term)" @default.
- Q55786282 description "seltene angeborene Erkrankung" @default.
- Q55786282 name "Koussef-Syndrom" @default.
- Q55786282 name "Kousseff syndrome" @default.
- Q55786282 name "syndrome de Kousseff" @default.
- Q55786282 type Item @default.
- Q55786282 label "Koussef-Syndrom" @default.
- Q55786282 label "Kousseff syndrome" @default.
- Q55786282 label "syndrome de Kousseff" @default.
- Q55786282 altLabel "Sacral meningocele-conotruncal heart defects syndrome" @default.
- Q55786282 prefLabel "Koussef-Syndrom" @default.
- Q55786282 prefLabel "Kousseff syndrome" @default.
- Q55786282 prefLabel "syndrome de Kousseff" @default.
- Q55786282 P1550 Q55786282-5A1FC408-17D4-45CB-8065-2EFAE588CB05 @default.
- Q55786282 P279 Q55786282-05E45EFD-EFFF-47E1-A5EA-18D41316A5B6 @default.
- Q55786282 P2888 Q55786282-2BE39FE5-19BC-4834-B99B-316E1362B3D9 @default.
- Q55786282 P2892 Q55786282-D1283A63-FA26-4504-8491-77969429F0D8 @default.
- Q55786282 P31 Q55786282-118803AA-7B7F-467B-8AEC-87E455FBF584 @default.
- Q55786282 P31 Q55786282-1307DBBD-D5EB-4557-AB7C-939020FECDDF @default.
- Q55786282 P4229 Q55786282-608D9C30-E75F-45B5-B1BA-ABF84ACB51F7 @default.
- Q55786282 P486 Q55786282-24769A39-1114-4B64-BA73-BC827B20AADA @default.
- Q55786282 P5270 Q55786282-E3A372A1-DFBC-4325-83A8-726AED75910C @default.
- Q55786282 P486 C537223 @default.
- Q55786282 P5270 MONDO_0016522 @default.
- Q55786282 P1550 "2351" @default.
- Q55786282 P279 Q55786835 @default.
- Q55786282 P2888 Orphanet_2351 @default.
- Q55786282 P2892 "C2931444" @default.
- Q55786282 P31 Q112193867 @default.
- Q55786282 P31 Q55788864 @default.
- Q55786282 P4229 "Q87.8" @default.
- Q55786282 P486 "C537223" @default.
- Q55786282 P5270 "MONDO_0016522" @default.