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414403008: Herniated structure (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2005. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2529715011 Herniated structure (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
2533146017 Hernia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2536927011 Herniated structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2536928018 Herniated tissue en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2536929014 Herniation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
814351000241112 hernie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

8 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Herniated structure (morphologic abnormality) Is a Protrusion true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Ischiorectal hernia with obstruction (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Paraumbilical hernia with obstruction Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Posterior perineal hernia (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 1
Recurrent right inguinal hernia with gangrene (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Recurrent left inguinal hernia with gangrene (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Obstructed recurrent left inguinal hernia with gangrene Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Obstructed recurrent right inguinal hernia with gangrene Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Obstructed bilateral inguinal hernia (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Obstructed left inguinal hernia with gangrene (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Right inguinal hernia with gangrene (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Obstructed left femoral hernia with gangrene (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Recurrent right femoral hernia with gangrene (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Obstructed left femoral hernia Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Obstructed right femoral hernia Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Obstructed recurrent left inguinal hernia (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Obstructed right inguinal hernia (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Obstruction co-occurrent and due to bilateral femoral hernia Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 4
Obstructed recurrent right femoral hernia (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Bilateral femoral hernia with gangrene Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Primary intra-abdominal hernia (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 1
Obstructed recurrent right femoral hernia with gangrene (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Bilateral recurrent femoral hernia (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Inguinosuperficial hernia Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 2
Herniation descends to scrotum Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 1
Beckwith-Wiedemann syndrome Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 1
Lumbar hernia with gangrene Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Obstructed recurrent left femoral hernia with gangrene Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Diaphragmatic hernia with gangrene Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Rolling hiatus hernia with gastric volvulus Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Parastomal hernia with gangrene Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 5
Basal encephalocele (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Lumbar hydromyelocele Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 3
Cervical hydromyelocele Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 3
Thoracic hydromyelocele Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 3
Temporal encephalocele Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Parietal encephalocele Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
A rare systemic disorder characterised by vitreoretinal and macular degeneration, as well as occipital encephalocele. Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 3
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by occipital atretic cephalocele associated with a specific facial dysmorphism (consisting of prominent forehead, narrow palpebral fissures, midface deficiency, narrow, malformed ears, broad nose and nasal root, grooved nasal tip and columella, laterally angulated, hypoplastic nares, short philtrum, thin upper lip, clift lip/palate, severe oligodontia, prominent chin) and large feet with sandal gap. Intellectual disability, developmental delay and hypoplastic finger and toenails have also been reported. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 5
Lethal occipital encephalocele-skeletal dysplasia syndrome is a rare, genetic, bone development disorder characterized by occipital and parietal bone hypoplasia leading to occipital encephalocele, calvarial mineralization defects, craniosynostosis, radiohumeral fusions, oligodactyly and other skeletal anomalies (arachnodactyly, terminal phalangeal aplasia of the thumbs, bilateral absence of the great toes, pronounced bilateral angulation of femora, shortened limbs, advanced osseous maturation). Fetal death in utero is associated. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 5
Meningoencephalocele Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 1
Cerebellar pressure cone Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Cervicothoracic spina bifida aperta with hydrocephalus Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Cervicothoracic spina bifida aperta Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Indirect left inguinal hernia Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Indirect bilateral inguinal hernias (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Indirect right inguinal hernia Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Direct bilateral inguinal hernias (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Lumbosacral spina bifida aperta Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Lumbosacral spina bifida aperta with hydrocephalus Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Thoracolumbosacral spina bifida aperta (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Thoracolumbosacral spina bifida aperta (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 5
Thoracolumbosacral spina bifida aperta (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 6
Spina bifida aperta of upper thoracic spine (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Spina bifida without hydrocephalus - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Thoracic spina bifida without hydrocephalus - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Lumbar spina bifida without hydrocephalus - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Sacral spina bifida without hydrocephalus - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Cervical spina bifida without hydrocephalus - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Irreducible ischiorectal hernia Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 4
Spina bifida with hydrocephalus - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 5
Cervical spina bifida with hydrocephalus - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 5
Lumbar spina bifida with hydrocephalus - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 1
Sacral spina bifida with hydrocephalus - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 5
Thoracic spina bifida with hydrocephalus - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Lumbosacral spina bifida aperta with hydrocephalus Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 7
Cervicothoracic spina bifida aperta with hydrocephalus Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 7
Rachischisis is a neural tube defect, which occurs when the neural folds do not join at the midline and the undifferentiated neuroectoderm remains exposed. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 1
Rachischisis is a neural tube defect, which occurs when the neural folds do not join at the midline and the undifferentiated neuroectoderm remains exposed. Rachischisis totalis (holorachischisis) is the extreme form in which the entire spinal cord remains open. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 1
Rachischisis with hydrocephalus Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 4
Rachischisis is a neural tube defect, which occurs when the neural folds do not join at the midline and the undifferentiated neuroectoderm remains exposed. Rachischisis partialis (merorachischisis) is the partial form where the spinal cord is partially closed and partially open. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
A rare closed neural tube defect characterized by cystic dilatation of the central canal of the spinal cord, herniating through a posterior vertebral arch defect (spina bifida) into an expanded cerebrospinal fluid (CSF) filled dural sac (meningocele). It can be located at the caudal part of the spinal cord (terminal myelocystocele) or above conus (non-terminal myelocystocele). Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Cervical myelocystocele Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Thoracic myelocystocele Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Lumbar myelocystocele Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Cervicothoracic spina bifida aperta Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 6
Lumbosacral spina bifida aperta Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
A type of spina bifida aperta that is usually caused by a vertebral defect associated with a superficial fatty mass (lipoma or fatty tumour) that merges with the lower level of the spinal cord. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Hemimyelocele Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Cervical myelocele Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 5
Cervical hydromyelocele Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 6
Thoracic hydromyelocele Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 6
Lumbar myelocele Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 5
Thoracic myelocele Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 5
Incisional hernia of anterior abdominal wall at trocar puncture site following laparoscopic procedure (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Iniencephaly - open Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
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. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Lethal hydranencephaly-diaphragmatic hernia syndrome is a rare, genetic, lethal, multiple congenital anomalies syndrome characterized by hydranencephaly and diaphragmatic hernia, as well as macrocephaly, a widely open anterior fontanel, scaphoid abdomen and hypotonia. Additionally, congenital heart defects, polyhydramnios and pulmonary hypertension have also been associated. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Posterior meningocele is a rare neural tube closure defect characterized by the herniation of a cerebrospinal fluid-filled sac, that is lined by dura and arachnoid mater, through a posterior spina bifida and covered by a layer of skin of variable thickness, which may be dysplastic or ulcerated. The spinal cord and nerves are generally not included and function normally, although sometimes a tethered cord may be associated. They are most commonly located in the lumbar or sacral region. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
A rare syndromic esophageal malformation characterized by severe congenital brachyesophagus with midline diaphragmatic hernia and secondary intrathoracic stomach, and vertebral anomalies (in particular rachischisis of the cervical/thoracic spine). Additional reported manifestations include intrauterine growth restriction, short neck, intestinal malrotation, herniation of other abdominal organs, and cleft lip, among others. The condition is mostly fatal in the neonatal or early infantile period. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 4
Secondary hernia of abdomen Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Rectocele - delivered with postpartum complication Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 1
Rectocele complicating postpartum care - baby delivered during previous episode of care Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 1
Rectocele - baby delivered Associated morphology False Herniated structure (morphologic abnormality) Inferred relationship Some 2
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by congenital diaphragmatic hernia, short bowel, and asplenia. Dysmorphic facial features include long forehead, hypertelorism, upturned nares, and small mandible. Atresia of the duodenum has also been reported. Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Meningoencephalocele of orbit (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Meningoencephalocele of orbit (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Congenital meningocele of orbit (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 2
Obstructed hernia of abdominal cavity Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Obstructed recurrent inguinal hernia (disorder) Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Obstructed recurrent femoral hernia Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 3
Paraesophageal hernia with gangrene AND obstruction Associated morphology True Herniated structure (morphologic abnormality) Inferred relationship Some 5

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