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93358007: Congenital malposition of testis (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
154514010 Congenital malposition of testis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
154515011 Congenital malpositioned testis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
837074017 Congenital malposition of testis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1882961000195115 malposizione testicolare congenita it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4710471000241114 malposition congénitale d'un testicule fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
434071000274116 Angeborene Hodenfehlstellung de Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


26 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital malposition of testis Is a Congenital anomaly of testis (disorder) true Inferred relationship Some
Congenital malposition of testis Occurrence Congenital false Inferred relationship Some
Congenital malposition of testis Associated morphology Congenital malposition false Inferred relationship Some 1
Congenital malposition of testis Course Multiple superficial injuries of lower leg false Inferred relationship Some
Congenital malposition of testis Finding site Testis structure false Inferred relationship Some 1
Congenital malposition of testis Finding site Entire genital organ (body structure) false Inferred relationship Some 1
Congenital malposition of testis Associated morphology anomalie du développement false Inferred relationship Some 2
Congenital malposition of testis Associated morphology anomalie du développement false Inferred relationship Some 2
Congenital malposition of testis Finding site Male genital structure false Inferred relationship Some 2
Congenital malposition of testis Finding site Genital structure false Inferred relationship Some 4
Congenital malposition of testis Associated morphology anomalie congénitale false Inferred relationship Some 4
Congenital malposition of testis Finding site Genital structure false Inferred relationship Some 2
Congenital malposition of testis Associated morphology Congenital malformation false Inferred relationship Some 2
Congenital malposition of testis Associated morphology Congenital malposition false Inferred relationship Some 2
Congenital malposition of testis Finding site Testis structure false Inferred relationship Some 2
Congenital malposition of testis Associated morphology anomalie congénitale false Inferred relationship Some 2
Congenital malposition of testis Finding site This structure, also termed the pelvic region, includes the wall, cavity and content of both the true and false pelvis; it consequently incorporates the entire bony pelvis; and inferiorly it is bounded and includes the pelvic diaphragm. The structure incorporates the complete pelvic wall; sacrococcygeal region (including the overlying skin and subcutaneous tissue); the contents of the false pelvic cavity; but in contrast to the 'pelvic segment of trunk' excludes the perineum, external genitalia. false Inferred relationship Some 2
Congenital malposition of testis Occurrence Congenital false Inferred relationship Some 2
Congenital malposition of testis Associated morphology anomalie du développement false Inferred relationship Some 3
Congenital malposition of testis Finding site Testis structure false Inferred relationship Some 3
Congenital malposition of testis Occurrence Congenital true Inferred relationship Some 1
Congenital malposition of testis Associated morphology Congenital malposition false Inferred relationship Some 1
Congenital malposition of testis Finding site Testis structure true Inferred relationship Some 1
Congenital malposition of testis Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Congenital malposition of testis Associated morphology Malposition (morphologic abnormality) true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital malposition of epididymis Is a False Congenital malposition of testis Inferred relationship Some
Undescended testicle Is a True Congenital malposition of testis Inferred relationship Some
Caudal appendage-deafness syndrome is characterized by caudal appendage, short terminal phalanges, deafness, cryptorchidism, intellectual deficit, short stature and dysmorphism. It has been described in monozygotic twin boys. Is a False Congenital malposition of testis Inferred relationship Some
Spigelian hernia-cryptorchidism syndrome is a rare developmental defect during embryogenesis characterized by a ventral, uni- or bilateral protrusion of extraperitoneal fat, peritoneum and/or intra-abdominal organs through a defect in the spigelian fascia (Spigelian hernia), associated with ipsi- 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. Is a False Congenital malposition of testis Inferred relationship Some

Reference Sets

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US English

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