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773623000: Spigelian hernia with cryptorchidism syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3724857010 Spigelian hernia with cryptorchidism syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3724858017 Spigelian hernia with cryptorchidism syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3724860015 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3724857010 Spigelian hernia with cryptorchidism syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3724858017 Spigelian hernia with cryptorchidism syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3724860015 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3431101001000114 Spieghel-Hernie-Kryptorchismus-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
875181000172117 syndrome de cryptorchidie-hernie de Spiegel fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
875181000172117 syndrome de cryptorchidie-hernie de Spiegel fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3431101001000114 Spieghel-Hernie-Kryptorchismus-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spigelian hernia with cryptorchidism syndrome (disorder) Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spigelian hernia with cryptorchidism syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Spigelian hernia with cryptorchidism syndrome (disorder) Finding site Structure of abdominopelvic viscus false Inferred relationship Existential restriction modifier (core metadata concept) 1
Spigelian hernia with cryptorchidism syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spigelian hernia with cryptorchidism syndrome (disorder) Finding site Structure of linea semilunaris (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Spigelian hernia with cryptorchidism syndrome (disorder) Is a Undescended testicle true Inferred relationship Existential restriction modifier (core metadata concept)
Spigelian hernia with cryptorchidism syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Spigelian hernia with cryptorchidism syndrome (disorder) Is a Gastroschisis (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Spigelian hernia with cryptorchidism syndrome (disorder) Is a Spigelian hernia true Inferred relationship Existential restriction modifier (core metadata concept)
Spigelian hernia with cryptorchidism syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Spigelian hernia with cryptorchidism syndrome (disorder) Associated morphology Congenital failure to migrate true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spigelian hernia with cryptorchidism syndrome (disorder) Finding site Testis structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spigelian hernia with cryptorchidism syndrome (disorder) Is a Congenital malposition of testis false Inferred relationship Existential restriction modifier (core metadata concept)
Spigelian hernia with cryptorchidism syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Spigelian hernia with cryptorchidism syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Spigelian hernia with cryptorchidism syndrome (disorder) Associated morphology Hernial opening (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Spigelian hernia with cryptorchidism syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Spigelian hernia with cryptorchidism syndrome (disorder) Is a Congenital anomaly of abdominal wall false Inferred relationship Existential restriction modifier (core metadata concept)
Spigelian hernia with cryptorchidism syndrome (disorder) Finding site Organ within abdominopelvic cavity false Inferred relationship Existential restriction modifier (core metadata concept) 1
Spigelian hernia with cryptorchidism syndrome (disorder) Finding site Structure of abdominopelvic cavity and/or content of abdominopelvic cavity and/or anterior abdominal wall (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Spigelian hernia with cryptorchidism syndrome (disorder) Is a Congenital malformation of anterior abdominal wall (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Spigelian hernia with cryptorchidism syndrome (disorder) Finding site Intra-abdominopelvic structure true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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