FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

18735004: Congenital omphalocele (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2020. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
31596019 Congenital omphalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
31597011 Omphalocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
746271010 Congenital omphalocele (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2535837011 Amniocele en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4598091000005111 kongenit omfalocele da Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Danish module (core metadata concept)


9 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital omphalocele Is a Kongenit abdominalvæganomali false Inferred relationship Some
Congenital omphalocele Associated morphology kongenit manglende sammenvoksning false Inferred relationship Some 2
Congenital omphalocele Associated morphology kongenit protrusion false Inferred relationship Some 1
Congenital omphalocele Finding site struktur af abdominalvæggen false Inferred relationship Some 2
Congenital omphalocele Occurrence Congenital false Inferred relationship Some
Congenital omphalocele Finding site Umbilical structure true Inferred relationship Some 2
Congenital omphalocele Is a Disorder of umbilicus (disorder) false Inferred relationship Some
Congenital omphalocele Is a Congenital malformation false Inferred relationship Some
Congenital omphalocele Is a Congenital umbilical defect false Inferred relationship Some
Congenital omphalocele Is a Umbilical hernia (disorder) true Inferred relationship Some
Congenital omphalocele Is a Gastroschisis false Inferred relationship Some
Congenital omphalocele Finding site Intestinal structure false Inferred relationship Some 1
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 1
Congenital omphalocele Associated morphology Herniated structure (morphologic abnormality) true Inferred relationship Some 1
Congenital omphalocele Is a Congenital anomaly of intestinal tract false Inferred relationship Some
Congenital omphalocele Is a Intestinal hernia false Inferred relationship Some
Congenital omphalocele Is a Kongenit abdominalvæganomali false Inferred relationship Some
Congenital omphalocele Is a Congenital malformation false Inferred relationship Some
Congenital omphalocele Finding site struktur af abdominalvæggen false Inferred relationship Some 3
Congenital omphalocele Finding site struktur af abdominalvæggen false Inferred relationship Some 4
Congenital omphalocele Associated morphology kongenit anomali false Inferred relationship Some 4
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 1
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 3
Congenital omphalocele Finding site struktur af abdominalvæggen false Inferred relationship Some 3
Congenital omphalocele Finding site struktur af abdominalvæggen false Inferred relationship Some 4
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) true Inferred relationship Some 2
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 3
Congenital omphalocele Associated morphology Herniated structure (morphologic abnormality) false Inferred relationship Some 5
Congenital omphalocele Finding site struktur af bughulen false Inferred relationship Some 5
Congenital omphalocele Occurrence Congenital false Inferred relationship Some 6
Congenital omphalocele Associated morphology dysgenese false Inferred relationship Some 6
Congenital omphalocele Finding site struktur af abdominalvæggen false Inferred relationship Some 6
Congenital omphalocele Associated morphology Hernial opening (morphologic abnormality) false Inferred relationship Some 4
Congenital omphalocele Finding site Umbilical structure false Inferred relationship Some 4
Congenital omphalocele Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Congenital omphalocele Occurrence Congenital true Inferred relationship Some 2
Congenital omphalocele Occurrence Congenital true Inferred relationship Some 1
Congenital omphalocele Finding site struktur indre abdominalt organ false Inferred relationship Some 1
Congenital omphalocele Finding site Any organ (viscera) contained within the abdominopelvic cavity. The abdominopelvic viscera includes stomach, small intestine, large intestine, spleen, kidneys, adrenal glands, pancreas, liver and gallbladder and the viscera within the true pelvic cavity including ovaries, uterus, prostate, urinary bladder and anal canal. false Inferred relationship Some 1
Congenital omphalocele Is a Abdominal organ finding false Inferred relationship Some
Congenital omphalocele Finding site This structure comprises the space and content within the boundaries of the abdominopelvic cavity but excludes the walls that define and enclose the space. Previously SNOMED CT used the word 'compartment' to describe structures comprising the cavity and content but FMA has used the same word to include cavity, content and wall. As a consequence, the preferred notation is intra-abdominopelvic structure as this more clearly excludes the 'wall' structures. The intra-abdominopelvic structure is bounded by, but excludes the following 'wall' structures: superiorly the thoracic diaphragm; inferiorly the pelvic diaphragm; anteriorly the anterior abdominal wall (including the lateral abdominal wall); and posteriorly the wall of the abdominal proper segment of trunk. The pelvic component consists of the cavity and content of the true pelvis, which is bounded by the pelvic wall. Note, the structures that form the boundaries are excluded. true Inferred relationship Some 1
Congenital omphalocele Is a Congenital umbilical hernia (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Gangrenous omphalocele Is a False Congenital omphalocele Inferred relationship Some
Omphalocele with obstruction Is a True Congenital omphalocele Inferred relationship Some
Navlesnorsbrok Is a False Congenital omphalocele Inferred relationship Some
Beckwith-Wiedemann syndrome Is a True Congenital omphalocele Inferred relationship Some
Uspecificeret umbilikalhernie Is a False Congenital omphalocele Inferred relationship Some
Hepatomphalocele Is a True Congenital omphalocele Inferred relationship Some
Omphalocele with gangrene Is a True Congenital omphalocele Inferred relationship Some
Omphalocele - irreducible Is a True Congenital omphalocele Inferred relationship Some
ukompliceret omfalocele Is a False Congenital omphalocele Inferred relationship Some
Shprintzen-Goldberg omphalocele syndrome is a very rare inherited malformation syndrome characterized by omphalocele, scoliosis, mild dysmorphic features (downslanted palpebral fissures, s-shaped eyelids and thin upper lip), laryngeal and pharyngeal hypoplasia and learning disabilities. Is a True Congenital omphalocele Inferred relationship Some
A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of omphalocele and cleft palate. Other reported features include cleft lip, bifid uvula, bilateral talipes equinovarus, bicornuate uterus, and hydrocephalus internus. The condition is lethal in infancy. Is a True Congenital omphalocele Inferred relationship Some
Familial omphalocele syndrome with facial dysmorphism is a rare genetic developmental defect during embryogenesis characterized by omphalocele associated with facial dysmorphism including flat face, short, upturned nose, long and wide philtrum and flattened maxillary arch and abnormalities of hands. Is a True Congenital omphalocele Inferred relationship Some
A rare multiple congenital anomalies/dysmorphic syndrome characterized by a large omphalocele containing liver and small intestine, diaphragmatic hernia, cardiovascular anomalies (e. g. aortic coarctation), variable limb malformations (including radioulnar synostosis, agenesis of the radius and/or thumb, generalized syndactyly, and numerical reduction of toes), and dysmorphic facial features. Additional reported manifestations are unilateral absence of umbilical artery, intestinal malrotation, hypoplastic ovaries, and unilateral renal agenesis, among others. The condition is mostly fatal in the neonatal period. Is a True Congenital omphalocele Inferred relationship Some
Repair of omphalocele Has focus True Congenital omphalocele Inferred relationship Some 2
Gross operation repair of omphalocele, first stage Has focus True Congenital omphalocele Inferred relationship Some 2
Gross operation repair of omphalocele, second stage Has focus True Congenital omphalocele Inferred relationship Some 2
Repair of omphalocele with prosthesis Has focus True Congenital omphalocele Inferred relationship Some 2
Repair of omphalocele with staged closure of prosthesis Has focus True Congenital omphalocele Inferred relationship Some 2
Repair of large omphalocele with prosthesis Has focus True Congenital omphalocele Inferred relationship Some 2

Reference Sets

GB English

US English

Back to Start