767811005: Lesion of face (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Head finding (finding)\Finding of head region\Finding of face\Disorder of face (disorder)\Lesion of face
\Head finding (finding)\Disorder of head (disorder)\Disorder of face (disorder)\Lesion of face

\Disease\Disorder of head (disorder)\Disorder of face (disorder)\Lesion of face

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Lesion of face	Is a	Finding of face	false	Inferred relationship	Some
Lesion of face	Finding site	Face structure	true	Inferred relationship	Some	1
Lesion of face	Associated morphology	Lesion (morphologic abnormality)	true	Inferred relationship	Some	1
Lesion of face	Is a	Disorder of face (disorder)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Fronto-malar faciosynostosis	Is a	True	Lesion of face	Inferred relationship	Some
Blister of face with infection	Is a	True	Lesion of face	Inferred relationship	Some
Fractured dental restoration	Is a	False	Lesion of face	Inferred relationship	Some
Abscess of face	Is a	True	Lesion of face	Inferred relationship	Some
Periodontal lesion due to traumatic occlusion	Is a	False	Lesion of face	Inferred relationship	Some
Dysplasia of cementum (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Patterson-Stevenson-Fontaine syndrome is a very rare variant of acrofacial dysostosis characterized by mandibulofacial dysostosis and limb anomalies.	Is a	True	Lesion of face	Inferred relationship	Some
Isolated congenital syngnathia is a very rare developmental defect during embryogenesis disorder characterized by varying degrees of congenital fusion (ranging from simple mucosal adhesions to extensive bony fusion) of mandible to maxilla that is not associated with any other malformations. Patients present with mouth opening limitation (which could range from severe to minimal restriction) that typically results in feeding, swallowing and/or respiratory difficulties which may lead to failure to thrive, malnutrition and/or temporomandibular joint ankylosis.	Is a	False	Lesion of face	Inferred relationship	Some
Mass of nasal sinus (finding)	Is a	False	Lesion of face	Inferred relationship	Some
Mandibuloacral dysostosis	Is a	True	Lesion of face	Inferred relationship	Some
X-linked mandibulofacial dysostosis is an extremely rare multiple congenital abnormality syndrome that is characterised by microcephaly, malar hypoplasia with downslanting palpebral fissures, highly arched palate, apparently low-set and protruding ears, micrognathia, short stature, bilateral hearing loss, and learning disability. Occasionally, additional features have been observed such as bilateral cryptorchidism, cardiac valvular lesions, body asymmetry, and pectus excavatum.	Is a	True	Lesion of face	Inferred relationship	Some
Congenital failure of fusion between maxillary and mandibular processes (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Byzanthine arch palate	Is a	True	Lesion of face	Inferred relationship	Some
Cleft of alveolar ridge (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Cleft mandible	Is a	True	Lesion of face	Inferred relationship	Some
Congenital macrostomia	Is a	True	Lesion of face	Inferred relationship	Some
Teebi-Shaltout syndrome is a rare, genetic, development defect during embryogenesis malformation syndrome characterized by association of characteristic facial features (including abnormal head shape with narrow forehead, hypertelorism, telecanthus, small earlobes, broad nasal bridge and tip, underdeveloped ala nasi, small/wide mouth and high/cleft palate), ectodermal dysplasia (including oligodontia with delayed dentition, slow growing hair and reduced sweating) and skeletal abnormalities including camptodactyly and caudal appendage. Short stature and abnormal palmar creases are additional clinical features.	Is a	True	Lesion of face	Inferred relationship	Some
Familial osteodysplasia, Anderson type is a rare, genetic dysostosis disorder characterized by craniofacial bone abnormalities (i.e. midface hypoplasia, broad, flat nasal bridge, narrow, thin prognathic mandible with pointed chin, malocclusion, partial dental agenesis) associated with additional osseous anomalies, including scoliosis, calvarial thinning, pointed spinous processes, clinodactyly and abnormal phalanges. Elevated erythrocyte sedimentation rate, hyperuricemia and hypertension have also been reported. There have been no further descriptions in the literature since 1982.	Is a	True	Lesion of face	Inferred relationship	Some
Mandibulofacial dysostosis-macroblepharon-macrostomia syndrome is a rare developmental defect during embryogenesis disorder characterized by macroblepharon, ectropion, and facial dysmorphism which includes severe hypertelorism, downslanting palpebral fissures, posteriorly rotated ears, broad nasal bridge, long and smooth philtrum, and macrostomia with thin upper lip vermilion border. Other features may include large fontanelles, prominent metopic ridge, thick eyebrows, mild synophrys, increased density of upper eyelashes, anteverted nares, abnormal dentition and capillary hemangioma.	Is a	True	Lesion of face	Inferred relationship	Some
Congenital abnormal fusion of lacrimal bone	Is a	True	Lesion of face	Inferred relationship	Some
Enamel spur	Is a	False	Lesion of face	Inferred relationship	Some
Exostosis of jaw toward buccal region (disorder)	Is a	False	Lesion of face	Inferred relationship	Some
Lingual exostosis	Is a	False	Lesion of face	Inferred relationship	Some
Labial exostosis	Is a	False	Lesion of face	Inferred relationship	Some
Torus palatinus	Is a	True	Lesion of face	Inferred relationship	Some
Exostosis of jaw	Is a	True	Lesion of face	Inferred relationship	Some
A rare multiple congenital defects/dysmorphic syndrome characterized by variable degrees of bony syngnathia associated with variable additional abnormalities, including growth retardation, intellectual disability, microcephaly, iris coloboma, nystagmus, deafness, and vertebral segmentation defects, as well as genital, limb and additional facial malformations, among others.	Is a	True	Lesion of face	Inferred relationship	Some
Tinea kerion of beard	Is a	False	Lesion of face	Inferred relationship	Some
Mass of preauricular region (finding)	Is a	False	Lesion of face	Inferred relationship	Some
An ectopic tooth that has erupted on the lingual aspect of the maxilla or mandible.	Is a	False	Lesion of face	Inferred relationship	Some
Posterior perimaxillary faciosynostosis	Is a	True	Lesion of face	Inferred relationship	Some
Polyp of ethmoidal sinus	Is a	False	Lesion of face	Inferred relationship	Some
Acquired stenosis of right nasolacrimal duct	Is a	True	Lesion of face	Inferred relationship	Some
Hypertelorism-hypospadias-polysyndactyly syndrome is a very rare syndrome associating an acro-fronto-facio-nasal dysostosis with genitourinary anomalies.	Is a	True	Lesion of face	Inferred relationship	Some
Polyp of sphenoidal sinus	Is a	False	Lesion of face	Inferred relationship	Some
Gingival and edentulous alveolar ridge lesion due to trauma (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Birth injury to face	Is a	True	Lesion of face	Inferred relationship	Some
Buccal pigmentation due to Addison's disease (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Segmental odontomaxillary dysplasia (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Goundou of yaws	Is a	False	Lesion of face	Inferred relationship	Some
Basal encephalocele (disorder)	Is a	False	Lesion of face	Inferred relationship	Some
Stafne idiopathic bone cavity of mandible	Is a	True	Lesion of face	Inferred relationship	Some
Periorbital ecchymosis	Is a	True	Lesion of face	Inferred relationship	Some
Ecchymosis of buccal mucosa	Is a	True	Lesion of face	Inferred relationship	Some
Crushing injury of face	Is a	True	Lesion of face	Inferred relationship	Some
Sprain of jaw	Is a	True	Lesion of face	Inferred relationship	Some
Avulsion of periorbital region	Is a	True	Lesion of face	Inferred relationship	Some
Avulsion of maxilla	Is a	True	Lesion of face	Inferred relationship	Some
Contusion of face	Is a	True	Lesion of face	Inferred relationship	Some
Fracture of ethmoid bone	Is a	False	Lesion of face	Inferred relationship	Some
Fracture of lacrimal bone	Is a	False	Lesion of face	Inferred relationship	Some
Osteoradionecrosis of facial bones	Is a	True	Lesion of face	Inferred relationship	Some
Frostbite of face	Is a	True	Lesion of face	Inferred relationship	Some
Open wound of face	Is a	True	Lesion of face	Inferred relationship	Some
Burn of face (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Superficial injury of face	Is a	True	Lesion of face	Inferred relationship	Some
Human bite of face	Is a	False	Lesion of face	Inferred relationship	Some
Avulsion of circumoral region of face	Is a	True	Lesion of face	Inferred relationship	Some
Strain of muscle of face	Is a	True	Lesion of face	Inferred relationship	Some
Animal bite of face	Is a	False	Lesion of face	Inferred relationship	Some
Injury of face and neck	Is a	True	Lesion of face	Inferred relationship	Some
Injury of meniscus of temporomandibular joint	Is a	False	Lesion of face	Inferred relationship	Some
Fracture of bone of face	Is a	True	Lesion of face	Inferred relationship	Some
Avulsion of cheek	Is a	True	Lesion of face	Inferred relationship	Some
Avulsion of forehead	Is a	True	Lesion of face	Inferred relationship	Some
Avulsion of mandible	Is a	True	Lesion of face	Inferred relationship	Some
Hemimaxillofacial dysplasia	Is a	True	Lesion of face	Inferred relationship	Some
A rare X-linked malformation syndrome characterized by craniofacial abnormalities such as uni- or bicoronal synostosis, hypertelorism and a bifid nose, grooved or split nails, frizzy hair, abnormalities of the shoulder girdle, hands and feet.	Is a	True	Lesion of face	Inferred relationship	Some
Multiple injuries of face	Is a	True	Lesion of face	Inferred relationship	Some
A rare mandibulofacial dysostosis characterized by the association with scalp alopecia and sparse eyebrows and eyelashes. Craniofacial dysmorphic features include zygomatic and mandibular dysplasia or hypoplasia, cleft palate, micrognathia, dental anomalies, auricular dysmorphism, and eyelid anomalies, among others. Patients may experience limited jaw mobility, glossoptosis, upper airway obstruction, and conductive hearing loss.	Is a	True	Lesion of face	Inferred relationship	Some
A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by craniofacial dysmorphism (including an abnormal skull shape, hypertelorism, downslanting palpebral fissures, epicanthal folds, low-set ears, depressed nasal bridge, micrognathia), short stature, ectodermal anomalies (such as sparse eyebrows, eyelashes, and scalp hair, hypoplastic toenails), developmental delay, and intellectual disability. Additional features may include cerebral/cerebellar malformations and mild renal involvement.	Is a	True	Lesion of face	Inferred relationship	Some
A rare osteonecrosis characterized by an exposed necrotic lesion in the mandible or maxilla present for more than eight weeks, arising as a complication of antiresorptive medication, dental interventions, or trauma and infections. Patients may present with pain, altered neurosensory functions, secondary infections, and (in advanced stages) pathological fractures, or fistulae.	Is a	True	Lesion of face	Inferred relationship	Some
A rare multiple congenital anomalies/dysmorphic syndrome with intellectual disability characterized by severe congenital contractures of the limbs and face, hypotonia, neonatal respiratory distress, and global developmental delay. Dysmorphic facial features include downslanting palpebral fissures, broad nasal bridge, large nares, long philtrum, and deep nasolabial folds, among others. Limb deformities (camptodactyly, clubfoot), short neck, scoliosis, as well as seizures have also been reported. Brain MRI may show cerebral and cerebellar atrophy in some cases.	Is a	True	Lesion of face	Inferred relationship	Some
Local exogenous pigmentation of left buccal mucosa	Is a	True	Lesion of face	Inferred relationship	Some
Local exogenous pigmentation of right buccal mucosa (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Bite wound of face (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Ectopic parotid gland tissue	Is a	True	Lesion of face	Inferred relationship	Some
Stenosis of parotid duct	Is a	True	Lesion of face	Inferred relationship	Some
Fistula of parotid gland	Is a	True	Lesion of face	Inferred relationship	Some
Parotid sialolithiasis	Is a	True	Lesion of face	Inferred relationship	Some
Lacrimal and parotid gland sarcoidosis	Is a	True	Lesion of face	Inferred relationship	Some
Parotid sialodocholithiasis	Is a	True	Lesion of face	Inferred relationship	Some
Asteroid hyalosis	Is a	True	Lesion of face	Inferred relationship	Some
Strabismus fixus	Is a	True	Lesion of face	Inferred relationship	Some
Avulsion of vitreous base	Is a	True	Lesion of face	Inferred relationship	Some
Aqueous humor misdirect (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Vitreous opacities (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Lymphangioma of orbit (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Entrapment of extraocular muscle (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Vitreoretinal dysplasia	Is a	True	Lesion of face	Inferred relationship	Some
Lesion of conjunctiva (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Vitreous detachment	Is a	True	Lesion of face	Inferred relationship	Some
Vitreoretinal adhesion (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
A rare syndromic disorder with strabismus with characteristics of congenital non-progressive ophthalmoplegia affecting the oculomotor and/or trochlear nucleus/nerve and their innervated muscles. Patients present with abnormal resting position of the eyes (in most cases infraducted and exotropic), limitation of vertical and horizontal gaze, impaired binocular vision, amblyopia, unilateral or bilateral blepharoptosis, and compensatory abnormal head posture. Extraocular manifestations include intellectual disability, peripheral neuropathy, and skeletal abnormalities among others.	Is a	True	Lesion of face	Inferred relationship	Some
Adhesion of extraocular muscle (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Cementum caries	Is a	True	Lesion of face	Inferred relationship	Some
Non-active cavitated caries of tooth root (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Active cavitated caries of tooth root (disorder)	Is a	True	Lesion of face	Inferred relationship	Some
Non-cavitated caries of tooth root	Is a	True	Lesion of face	Inferred relationship	Some
Primary dental caries, root surface origin	Is a	True	Lesion of face	Inferred relationship	Some
Concussion of periodontal ligament	Is a	True	Lesion of face	Inferred relationship	Some

Start Page 2 of 3 End

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3675596018	Lesion of face	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3675597010	Facial lesion	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
5069427016	Lesion of face (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6006981000241110	lésion du visage	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6006991000241112	lésion de la face	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module
6007001000241117	lésion faciale	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module