Congenital spinal meningocele	congenitale afwijking van hart	congenitale sacrale meningocele	malformatiesyndroom met betrokkenheid van meerdere systemen
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syndroom van congenitale sacrale meningocele met conotruncaal hartdefect (aandoening)
	syndroom van congenitale sacrale meningocele met conotruncaal hartdefect
	Kousseff-syndroom syndroom van Kousseff aangeboren syndroom van sacrale meningokèle met conotruncale hartafwijking
	Kousseff syndrome
	Congenital sacral meningocele with conotruncal heart defect syndrome
	A rare syndromic central nervous system malformation characterized by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11.

Id	726083008
Status	Primitive

Associated morphology	herniatie
Finding site	structuur van meningen van pars sacralis medullae spinalis
Occurrence	congenitaal

Associated morphology	morfologische afwijking
Finding site	structuur van hart
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	fusiedefect door stoornis in ontwikkeling
Finding site	structuur van arcus vertebrae
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

DHD Diagnosis thesaurus reference set

RIVM authorized national diagnosis thesaurus to ICD10 complex mapping reference set

Target	Q87.8
Term	Overige gespecificeerde congenitale gestoorde-ontwikkelingssyndromen, niet elders geclassificeerd

SNOMED CT to Orphanet simple map

2351

SNOMED CT to ICD-10 extended map

Target	Q87.8
Rule	TRUE
Advice	ALWAYS Q87.8 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified