congenitale afwijking van voorwand van buik	hernia Spigelii	malformatiesyndroom met betrokkenheid van meerdere systemen	niet-ingedaalde testis
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syndroom van hernia Spigelii met cryptorchisme (aandoening)
	syndroom van hernia Spigelii met cryptorchisme
	syndroom van hernia van Spiegel met niet-ingedaalde testis
	Spigelian hernia with cryptorchidism syndrome
	A rare developmental defect during embryogenesis with characteristics of ventral, unilateral or bilateral protrusion of extraperitoneal fat, peritoneum and/or intra-abdominal organs through a defect in the spigelian fascia (spigelian hernia), associated with ipsilateral or bilateral undescended testis (usually found within or just beneath the hernial sac) in male neonates. The gubernaculum and/or inguinal canal may be absent.

Id	773623000
Status	Primitive

Associated morphology	herniatie
Finding site	structuur van abdominopelviene holte en/of inhoud
Occurrence	congenitaal

Associated morphology	congenitaal migratiedefect
Finding site	structuur van testis
Occurrence	congenitaal
Pathological process	proces van pathologische ontwikkeling

Associated morphology	breukpoort
Finding site	lijn van Spigelius
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	K43.6
Term	Overige en niet gespecificeerde hernia ventralis met obstructie, zonder gangreen

Target	Q53.9
Term	Niet ingedaalde testis, niet gespecificeerd

SNOMED CT to Orphanet simple map

314432

SNOMED CT to ICD-10 extended map

Target	K43.6
Rule	TRUE
Advice	ALWAYS K43.6 \| POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
Correlation	SNOMED CT source code to target map code correlation not specified

Target	Q53.9
Rule	TRUE
Advice	ALWAYS Q53.9
Correlation	SNOMED CT source code to target map code correlation not specified