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112639008: Protrusion (morphologic abnormality)

Status: current, Not 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
183288018 Protrusion en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
190371012 Evagination en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
642112018 Protrusion (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

21 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Protrusion Is a Mechanical abnormality true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital meningocele Associated morphology False Protrusion Inferred relationship Some 1
Postoperative meningocele Associated morphology False Protrusion Inferred relationship Some 1
Traumatic meningocele Associated morphology False Protrusion Inferred relationship Some 1
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 False Protrusion Inferred relationship Some 1
Lateral meningocele Associated morphology False Protrusion Inferred relationship Some 1
Meningomyelocele of lumbosacral spine (disorder) Associated morphology False Protrusion Inferred relationship Some 3
Meningocele of vertex (disorder) Associated morphology False Protrusion Inferred relationship Some 1
Meningomyelocele (disorder) Associated morphology False Protrusion Inferred relationship Some 1
Meningomyelocele (disorder) Associated morphology False Protrusion Inferred relationship Some 1
Meningomyelocele of lumbosacral spine (disorder) Associated morphology False Protrusion Inferred relationship Some 3
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 False Protrusion Inferred relationship Some 1
Congenital meningocele Associated morphology False Protrusion Inferred relationship Some 1
Acquired meningocele Associated morphology False Protrusion Inferred relationship Some 1
Meningocele of vertex (disorder) Associated morphology False Protrusion Inferred relationship Some 1
Meningocele Associated morphology False Protrusion Inferred relationship Some 1
Postoperative meningocele Associated morphology False Protrusion Inferred relationship Some 1
Meningocele - cranial Associated morphology False Protrusion Inferred relationship Some 1
Traumatic meningocele Associated morphology False Protrusion Inferred relationship Some 1
Lateral meningocele Associated morphology False Protrusion Inferred relationship Some 1
Meningocele - cerebral Associated morphology False Protrusion Inferred relationship Some 1
Known OR suspected fetal spina bifida with myelomeningocele affecting obstetrical care Associated morphology False Protrusion Inferred relationship Some 3
Myelomeningocele without hydrocephalus (disorder) Associated morphology False Protrusion Inferred relationship Some 4
Lipomyelomeningocele Associated morphology False Protrusion Inferred relationship Some 8
Exstrophy of cloaca sequence Associated morphology False Protrusion Inferred relationship Some 8
Exstrophy of cloaca sequence Associated morphology True Protrusion Inferred relationship Some 5
Exstrophy of cloaca sequence Associated morphology False Protrusion Inferred relationship Some 9
Exstrophy of cloaca sequence Associated morphology True Protrusion Inferred relationship Some 6
Congenital sacral meningocele Associated morphology False Protrusion Inferred relationship Some 6
Myelomeningocele co-occurrent with hydrocephalus (disorder) Associated morphology False Protrusion Inferred relationship Some 6
Myelomeningocele co-occurrent with hydrocephalus (disorder) Associated morphology False Protrusion Inferred relationship Some 10
Protrusive upper lip Associated morphology True Protrusion Inferred relationship Some 1
Protrusive lower lip Associated morphology True Protrusion Inferred relationship Some 1
Myelomeningocele co-occurrent with hydrocephalus (disorder) Associated morphology False Protrusion Inferred relationship Some 4
Myelomeningocele co-occurrent with hydrocephalus (disorder) Associated morphology False Protrusion Inferred relationship Some 3
Congenital tracheocele Associated morphology True Protrusion Inferred relationship Some 1
Hydrencephalomeningocele Associated morphology False Protrusion Inferred relationship Some 2
Mandibular prognathism Associated morphology True Protrusion Inferred relationship Some 1
hydroméningocèle Associated morphology False Protrusion Inferred relationship Some 2
The MMEP syndrome is a congenital syndromic form of split-hand/foot malformation. It is characterized by microcephaly, microphthalmia, ectrodactyly of the lower limbs and prognathism. Intellectual deficit has been reported. MMEP syndrome is considered to be a very rare condition, although the exact prevalence remains unknown. The etiology is not completely understood. Disruption of the sorting nexin 3 gene (SNX3; 6q21) has been shown to play a causative role in MMEP, although this was not confirmed in recent studies. Associated morphology True Protrusion Inferred relationship Some 3
hydroméningocèle crânienne congénitale Associated morphology False Protrusion Inferred relationship Some 3
Maxillary prognathism Associated morphology True Protrusion Inferred relationship Some 1
Congenital prognathism Associated morphology True Protrusion Inferred relationship Some 1
A rare, genetic, developmental defect during embryogenesis disorder characterized by abnormal forward projection of the mandible beyond the standard relation to the cranial base, with lower incisors often overlapping the upper incisors, that is inherited in an autosomal dominant manner. Association with mildly everted lower eyelids, flat malar area, thickened lower lip and craniosynostosis has been reported. Associated morphology True Protrusion Inferred relationship Some 1
Protrusion of tooth (finding) Associated morphology True Protrusion Inferred relationship Some 1
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. Associated morphology True Protrusion Inferred relationship Some 1
Myelocele with hydrocephalus (disorder) Associated morphology False Protrusion Inferred relationship Some 5
hydromyélocèle Associated morphology False Protrusion Inferred relationship Some 2
Congenital protrusion of tongue Associated morphology True Protrusion Inferred relationship Some 1
A rare syndromic central nervous system malformation characterized by the association of conotruncal heart defects, myelomeningocele and craniofacial dysmorphism similar to that seen in monosomy 22q11. Associated morphology False Protrusion Inferred relationship Some 1
Thoracic myelocele Associated morphology False Protrusion Inferred relationship Some 1
Repair of lipomeningocele (procedure) Direct morphology True Protrusion Inferred relationship Some 1
Dens evaginatus Associated morphology True Protrusion Inferred relationship Some 1
A rare disorder that presents as a flat neural placode (at the level of the skin of the back) that is exposed to the environment. The lack of expansion of the subarachnoid space distinguishes this lesion from myelomeningocele. Associated morphology False Protrusion Inferred relationship Some 1
Cervical hydromyelocele Associated morphology False Protrusion Inferred relationship Some 1
Lumbar hydromyelocele Associated morphology False Protrusion Inferred relationship Some 1
Meningomyelocele of lumbosacral spine (disorder) Associated morphology False Protrusion Inferred relationship Some 6
Thoracic hydromyelocele Associated morphology False Protrusion Inferred relationship Some 1
Hydromyelocele with hydrocephalus Associated morphology False Protrusion Inferred relationship Some 2
Laryngotomy with removal of laryngocele Direct morphology True Protrusion Inferred relationship Some 2
Acquired myelocele Associated morphology True Protrusion Inferred relationship Some 2
Tracheocele Associated morphology True Protrusion Inferred relationship Some 1
Encephalomyelocele Associated morphology True Protrusion 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 False Protrusion Inferred relationship Some 2
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 False Protrusion Inferred relationship Some 3
Cervical myelocele Associated morphology False Protrusion Inferred relationship Some 2
Lumbar myelocele Associated morphology False Protrusion Inferred relationship Some 2
Thoracic myelocele Associated morphology False Protrusion Inferred relationship Some 2
Cervical hydromyelocele Associated morphology False Protrusion Inferred relationship Some 3
Thoracic hydromyelocele Associated morphology False Protrusion Inferred relationship Some 3
Characterized by upper and lower incisors that have emerged forward making the teeth and lips protrude. Associated morphology True Protrusion Inferred relationship Some 2
Characterized by upper and lower incisors that have emerged forward making the teeth and lips protrude. Associated morphology True Protrusion Inferred relationship Some 3
Protrusion of prosthetic breast implant (disorder) Associated morphology True Protrusion Inferred relationship Some 1
Osteotomy of mandible and retrusion of mandible Direct morphology True Protrusion Inferred relationship Some 2
X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome is a rare syndromic intellectual disability characterized by hypotonia, microcephaly, severe developmental delay, seizures, intellectual disability, growth retardation, cardiac septal defects, cryptorchidism, hypospadias, and dysmorphic features - prominent ears, prognathism, thin upper lip, dental crowding. Associated morphology True Protrusion Inferred relationship Some 1
Protrusion of intraocular lens Associated morphology True Protrusion Inferred relationship Some 2
Protrusion of cardiac device Associated morphology True Protrusion Inferred relationship Some 1
A rare genetic multiple congenital anomalies/dysmorphic syndrome characterized by the association of severe intellectual disability, strabismus, and anterior maxillary protrusion with vertical maxillary excess, open bite, and prominent crowded teeth. Mild cochlear hearing loss has been reported in addition. Associated morphology True Protrusion Inferred relationship Some 1
Acquired keratoglobus Associated morphology True Protrusion Inferred relationship Some 2
Congenital keratoglobus Associated morphology True Protrusion Inferred relationship Some 2
Keratoglobus (disorder) Associated morphology True Protrusion Inferred relationship Some 1
Intrapelvic protrusion of right acetabulum (disorder) Associated morphology True Protrusion Inferred relationship Some 1
Intrapelvic protrusion of left acetabulum (disorder) Associated morphology True Protrusion Inferred relationship Some 1
Protrusion of bone Associated morphology True Protrusion Inferred relationship Some 1
Intrapelvic protrusion of acetabulum of bilateral hips Associated morphology True Protrusion Inferred relationship Some 1
Intrapelvic protrusion of acetabulum of bilateral hips Associated morphology True Protrusion Inferred relationship Some 2
Prominent forehead (finding) Associated morphology True Protrusion Inferred relationship Some 1

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