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Spigelian hernia with cryptorchidism syndrome (disorder)
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.
syndroom van hernia Spigelii met cryptorchisme
syndroom van hernia van Spiegel met niet-ingedaalde testis
Id773623000
StatusPrimitive
Associated morphologyHernia
Finding siteAbdomen
OccurrenceCongenital
Associated morphologyCongenital failure to migrate
Finding siteTestis structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyHernial opening
Finding siteLinea semilunaris
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetK43.6
RuleTRUE
AdviceALWAYS K43.6 | POSSIBLE REQUIREMENT FOR ADDITIONAL CODE TO FULLY DESCRIBE DISEASE OR CONDITION
CorrelationSNOMED CT source code to target map code correlation not specified
TargetQ53.9
RuleTRUE
AdviceALWAYS Q53.9
CorrelationSNOMED CT source code to target map code correlation not specified