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), associa
syndrome de cryptorchidie-hernie de Spiegel
SNOMEDCT-BE (spigelian hernia), associa / 773623000
SNOMEDCT-BE (disorder) / 773623000