38199008: Tooth structure (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary).\Digestive organ structure\Tooth structure

\Body system structure\Structure of digestive system (body structure)\...

\Entire digestive tract including mouth, esophagus, stomach and intestines.\Digestive tract part (body structure)\Upper digestive tract structure\Structure of mouth and/or pharynx\Mouth region structure\Mouth region part\Structure of internal part of mouth\...

\Oral hard tissue structure\Tooth structure

\Tooth, gum, and/or supporting structure (body structure)\Tooth structure

\Digestive organ structure\Tooth structure

\Body tissue structure (body structure)\Oral hard tissue structure\Tooth structure

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Tooth structure	Is a	Oral hard tissue structure	true	Inferred relationship	Some
Tooth structure	Is a	Digestive organ structure	false	Inferred relationship	Some
Tooth structure	Is a	Tooth, gum, and/or supporting structure (body structure)	true	Inferred relationship	Some
Tooth structure	del af	All teeth, gums and supporting structures	false	Inferred relationship	Some
Tooth structure	Is a	Digestive organ structure	true	Inferred relationship	Some
Tooth structure	del af	Entire oral cavity	false	Additional relationship	Some
Tooth structure	del af	Entire face	false	Additional relationship	Some
Tooth structure	Is a	Oral cavity structure	false	Inferred relationship	Some
Tooth structure	del af	Entire gastrointestinal tract	false	Additional relationship	Some
Tooth structure	Is a	Structure of half of head lateral to midsagittal plane (body structure)	true	Inferred relationship	Some
Tooth structure	Laterality	Side	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Completely impacted tooth in bone	Finding site	False	Tooth structure	Inferred relationship	Some	2
Impacted tooth in soft tissue	Finding site	False	Tooth structure	Inferred relationship	Some	2
Impacted permanent canine tooth	Finding site	False	Tooth structure	Inferred relationship	Some	2
Root angulation of tooth (disorder)	Finding site	False	Tooth structure	Inferred relationship	Some	2
Partially impacted tooth in bone	Finding site	False	Tooth structure	Inferred relationship	Some	2
Complicated impacted tooth	Finding site	False	Tooth structure	Inferred relationship	Some	2
Reverse position of adjacent teeth (disorder)	Finding site	False	Tooth structure	Inferred relationship	Some	2
Nonsupernumerary impacted tooth	Finding site	False	Tooth structure	Inferred relationship	Some	2
Impakterede tænder med abnorm position	Finding site	False	Tooth structure	Inferred relationship	Some	2
Impacted third molar tooth	Finding site	False	Tooth structure	Inferred relationship	Some	2
A genetic transmission deafness syndrome. The profound congenital deafness is associated with a complete absence of inner ear structures (Michel aplasia) microtia type I with small auricle and narrow external auditory canal and microdontia with widely spaced teeth. Linkage analysis followed by sequencing of candidate genes led to identification of three different homozygous mutations in the FGF3 gene (11q13). Transmission is autosomal recessive.	Finding site	False	Tooth structure	Inferred relationship	Some	5
Rotation of tooth	Finding site	False	Tooth structure	Inferred relationship	Some	3
Odontotomy	Procedure site - Direct (attribute)	True	Tooth structure	Inferred relationship	Some	1
Precocious exfoliation of teeth due to root resorption following trauma (disorder)	Finding site	False	Tooth structure	Inferred relationship	Some	4
Schinzel-Giedion syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Robinson nail dystrophy-deafness syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	6
Hypohidrotic X-linked ectodermal dysplasia	Finding site	True	Tooth structure	Inferred relationship	Some	3
Roselli-Gulienetti ectodermal dysplasia	Finding site	True	Tooth structure	Inferred relationship	Some	3
Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia	Finding site	True	Tooth structure	Inferred relationship	Some	3
Basan syndrome (disorder)	Finding site	True	Tooth structure	Inferred relationship	Some	3
Greither type of ectodermal dysplasia	Finding site	True	Tooth structure	Inferred relationship	Some	3
Anonychia with bizarre flexural pigmentation	Finding site	True	Tooth structure	Inferred relationship	Some	2
Tricho-onychodental dysplasia	Finding site	True	Tooth structure	Inferred relationship	Some	3
Schoepf-Schulz-Passage syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Odonto-onychial dysplasia with alopecia	Finding site	True	Tooth structure	Inferred relationship	Some	5
Fried's tooth and nail syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Dermodental dysplasi	Finding site	False	Tooth structure	Inferred relationship	Some	3
Salamon's syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Ectodermal dysplasia, syndactyly and pili torti	Finding site	True	Tooth structure	Inferred relationship	Some	3
Dwarfism, alopecia, pseudoanodontia, cutis laxa	Finding site	True	Tooth structure	Inferred relationship	Some	3
Hypohidrosis-diabetes insipidus syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	7
Odontotrichomelic syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	2
Berlin syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Dentookulokutant syndrom	Finding site	False	Tooth structure	Inferred relationship	Some	3
Sandman-Andra syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Flynn-Aird syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Curry-Hall syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Trichodental syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Cranioectodermal dysplasia	Finding site	True	Tooth structure	Inferred relationship	Some	4
Ectodermal dysplasia with hair-tooth-nail-sweating defect (disorder)	Finding site	True	Tooth structure	Inferred relationship	Some	2
Ectodermal dysplasia with hair-tooth-nail defects	Finding site	True	Tooth structure	Inferred relationship	Some	2
Ectodermal dysplasia with hair-tooth defects	Finding site	True	Tooth structure	Inferred relationship	Some	2
Ectodermal dysplasia with tooth-nail defects	Finding site	True	Tooth structure	Inferred relationship	Some	3
Ectodermal dysplasia with tooth-sweating defect	Finding site	True	Tooth structure	Inferred relationship	Some	3
Marshall syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	5
Oculodentodigital syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	6
Tricho-dento-osseous syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Ectrodactyly-ectodermal dysplasia-clefting syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	8
Root stunting (disorder)	Finding site	False	Tooth structure	Inferred relationship	Some	2
Hypoplastic enamel-onycholysis-hypohidrosis syndrome (disorder)	Finding site	True	Tooth structure	Inferred relationship	Some	3
Odonto-onycho-dermal dysplasia (disorder)	Finding site	True	Tooth structure	Inferred relationship	Some	3
Odontomicronychial ectodermal dysplasia (disorder)	Finding site	True	Tooth structure	Inferred relationship	Some	3
Ectodermal dysplasia with tooth-nail-sweating defect (disorder)	Finding site	True	Tooth structure	Inferred relationship	Some	3
Ectodermal syndrome with hair-tooth-sweating defects (disorder)	Finding site	True	Tooth structure	Inferred relationship	Some	2
Chondroectodermal dysplasia	Finding site	True	Tooth structure	Inferred relationship	Some	4
Hay-Wells syndrome of ectodermal dysplasia	Finding site	True	Tooth structure	Inferred relationship	Some	2
Anhidrotic ectodermal dysplasia with immune deficiency (disorder)	Finding site	True	Tooth structure	Inferred relationship	Some	6
Johanson-Blizzard syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	3
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	4
A rare malformation syndrome characterized by generalized multiple steatocystomas and natal teeth.	Finding site	True	Tooth structure	Inferred relationship	Some	1
Tricho-retino-dento-digital syndrome is an autosomal dominant ectodermal dysplasia syndrome, characterized by uncombable hair syndrome, congenital hypotrichosis and dental abnormalities such as oligodontia or hyperdontia, and associated with early-onset cataract, retinal pigmentary dystrophy, and brachydactyly with brachymetacarpia. Furthermore, hyperactivity and a mild intellectual deficit have been reported in affected patients.	Finding site	True	Tooth structure	Inferred relationship	Some	3
A rare ectodermal dysplasia syndrome characterized by severe arthrogryposis, multiple ectodermal dysplasia features, cleft lip/palate, facial dysmorphism, growth deficiency and a moderate delay of psychomotor development. Ectodermal dysplasia manifestations include sparse, brittle and hypopigmented hair, xerosis, multiple nevi, small conical shaped teeth and hypodontia, and facial dysmorphism with blepharophimosis, deep-set eyes and micrognathia.	Finding site	True	Tooth structure	Inferred relationship	Some	2
A rare genetic disease characterized by sensorineural hearing loss, abnormalities in the secondary dentition (such as enamel hypoplasia, taurodontism, or dental overcrowding), and nail abnormalities (including leukonychia and presence of transverse ridges). Association with macular dystrophy has also been reported.	Finding site	False	Tooth structure	Inferred relationship	Some	6
A rare genetic disease characterized by infantile onset of recurrent skin ulcerations, arthralgias, fever, peri-articular fistulous osteolysis, oligodontia, nail dystrophy, and keratitis. The disease takes a self-limiting course in childhood but results in severe cicatrization, chronic arthroses, pseudoacromegalic appearance of hands and feet, secondary scoliosis, and visual impairment. There have been no further descriptions in the literature since 1983.	Finding site	True	Tooth structure	Inferred relationship	Some	5
A rare ectodermal dysplasia syndrome characterized by a variably severe clinical picture comprising dry, thin skin, onychodysplasia, trichodysplasia, and dental abnormalities (such as hypodontia, microdontia, and persistence of deciduous teeth). There have been no further descriptions in the literature since 1990.	Finding site	True	Tooth structure	Inferred relationship	Some	2
A rare multiple congenital anomalies/dysmorphic syndrome characterized by intellectual disability, severe visual impairment due to ocular malformations (microphthalmos and microcornea with sclerocornea), short stature, hypotrichosis, dental anomalies, and dysmorphic facial features (such as a narrow nasal bridge with marked distal flaring and low-set, protruding ears). There have been no further descriptions in the literature since 1992.	Finding site	True	Tooth structure	Inferred relationship	Some	5
A rare, genetic, multiple congenital anomalies syndrome characterized by growth retardation, alopecia, pseudoanodontia and ocular manifestations.	Finding site	False	Tooth structure	Inferred relationship	Some	5
A rare multiple congenital anomalies/dysmorphic syndrome characterized by short stature and particularly pronounced shortening of the third to fifth metacarpals and metatarsals, congenital anodontia, sparse hair, dyspigmentation of the skin, hypoplastic nipples and underdeveloped external genitals in females, and multiple ocular abnormalities (such as distichiasis, strabismus, nystagmus, lenticular opacities, and severe myopia, among others). Dysmorphic craniofacial features include brachycephaly, downslanting palpebral fissures, broad nasal root, low-set ears, and small maxilla and prominent mandible. There have been no further descriptions in the literature since 1968.	Finding site	True	Tooth structure	Inferred relationship	Some	3
A rare ectodermal dysplasia syndrome characterized by bilateral retinitis pigmentosa, trichodysplasia (generalized hypotrichosis, structural changes), dental anomalies, onychodysplasia, and dry and scaly skin. There have been no further descriptions in the literature since 1988.	Finding site	True	Tooth structure	Inferred relationship	Some	4
A rare autosomal dominant ectodermal dysplasia syndrome characterized by premolar aplasia, hyperhidrosis, and premature graying of the hair. Additional features may include a narrow palate, hypoplastic nails, eyebrow anomalies, a unilateral simian crease, and poorly formed dermatoglyphics.	Finding site	True	Tooth structure	Inferred relationship	Some	3
A rare, genetic, ectodermal dysplasia syndrome characterized by corneal epithelial changes (ranging from roughening to nodular irregularities), diffuse palmoplantar hyperkeratosis with thickened, erythematous, scaly lesions affecting the elbows, knees and knuckles, distal onycholysis, brachydactyly accompanied by a single transverse palmar crease, short stature, premature birth, and increased susceptibility to tooth decay. Ocular symptoms include photophobia, reduced night vision, burning and watery eyes, and varying visual acuity. There have been no further descriptions in the literature since 1984.	Finding site	True	Tooth structure	Inferred relationship	Some	5
A rare genetic development defect during embryogenesis malformation syndrome with the 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.	Finding site	True	Tooth structure	Inferred relationship	Some	4
Chondroectodermal dysplasia with night blindness is a rare genetic bone development disorder characterized by proportionate short stature, nail dysplasia (enlarged, convex, hypertrophic nails), hypodontia and night blindness. Osteopenia, a tendency to present fractures, talipes varus with abnormal gait, ear infections, and watering eyes due to narrow tear ducts are frequently associated. Radiologically patients present delayed bone age on wrist X-rays, platyspondyly, and broad metaphyses of humeri with dense and thickened growth plates.	Finding site	True	Tooth structure	Inferred relationship	Some	5
Conductive deafness-ptosis-skeletal anomalies syndrome is a rare, genetic ectodermal dysplasia syndrome characterized by conductive hearing loss due to atresia of the external auditory canal and the middle ear complicated by chronic infection, ptosis and skeletal anomalies (internal rotation of hips, dislocation of the radial heads and fifth finger clinodactyly). In addition, a thin, pinched nose, delayed hair growth and dysplastic teeth are associated. There have been no further descriptions in the literature since 1978.	Finding site	False	Tooth structure	Inferred relationship	Some	4
Curly hair-acral keratoderma-caries syndrome is an extremely rare ectodermal dysplasia syndrome characterized by premature loss of curly, brittle, dry hair, premature loss of teeth due to caries, nail dystrophy with thickening of the finger- and toenails, acral keratoderma and hypohidrosis. Additionally, sparse eyebrows and eyelashes, receding frontal hairline and flattened malar region are associated. The severity of features appears to increase with age.	Finding site	True	Tooth structure	Inferred relationship	Some	3
Hallermann-Streiff syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	1
A rare genetic developmental defect during embryogenesis syndrome with characteristics of camptodactyly, joint contractures with amyotrophy, and ectodermal anomalies (oligodontia, enamel abnormalities, longitudinally broken nails, hypohidrotic skin with tendency to excessive bruising and scarring after injuries and scratching), as well as growth retardation, kyphoscoliosis, mild facial dysmorphism and microcephaly. There have been no further descriptions in the literature since 1992.	Finding site	True	Tooth structure	Inferred relationship	Some	2
Rinsing of mouth using fluoride treatment	Procedure site - Indirect (attribute)	True	Tooth structure	Inferred relationship	Some	1
Placement of orthodontic bracket using partial bonding	Procedure site - Indirect (attribute)	True	Tooth structure	Inferred relationship	Some	1
Placement of orthodontic traction chain (procedure)	Procedure site - Indirect (attribute)	True	Tooth structure	Inferred relationship	Some	1
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome	Finding site	True	Tooth structure	Inferred relationship	Some	1
Insertion of composite restoration using strip crown	Procedure site - Direct (attribute)	False	Tooth structure	Inferred relationship	Some	2
Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism	Finding site	False	Tooth structure	Inferred relationship	Some	3
Tapered teeth (disorder)	Finding site	False	Tooth structure	Inferred relationship	Some	1
Single tooth macrodontia (disorder)	Finding site	False	Tooth structure	Inferred relationship	Some	3
A genetic transmission deafness syndrome. The profound congenital deafness is associated with a complete absence of inner ear structures (Michel aplasia) microtia type I with small auricle and narrow external auditory canal and microdontia with widely spaced teeth. Linkage analysis followed by sequencing of candidate genes led to identification of three different homozygous mutations in the FGF3 gene (11q13). Transmission is autosomal recessive.	Finding site	False	Tooth structure	Inferred relationship	Some	6
A contiguous gene syndrome comprising otodental syndrome (characterized by globodontia and sensorineural high-frequency hearing deficit) associated with eye abnormalities including, typically, iris and chorioretinal coloboma, as well as, on occasion, microcornea, microphthalmos, lenticular opacity, lens coloboma and iris pigment epithelial atrophy.	Finding site	False	Tooth structure	Inferred relationship	Some	6
Fusion of mandibular incisor teeth (disorder)	Finding site	False	Tooth structure	Inferred relationship	Some	2
Taurodontism	Finding site	False	Tooth structure	Inferred relationship	Some	1
Amelogenesis imperfecta, hypomaturation hypoplasia type with taurodontism	Finding site	True	Tooth structure	Inferred relationship	Some	2
Hypotaurodontism (disorder)	Finding site	True	Tooth structure	Inferred relationship	Some	2
Mesotaurodontism	Finding site	False	Tooth structure	Inferred relationship	Some	1
Hypertaurodontism	Finding site	False	Tooth structure	Inferred relationship	Some	1
Relative generalised microdontia	Finding site	False	Tooth structure	Inferred relationship	Some	2
Segmental odontomaxillary dysplasia (disorder)	Finding site	True	Tooth structure	Inferred relationship	Some	2
Pain on tooth percussion	Finding site	True	Tooth structure	Inferred relationship	Some	2
Pulp vitality test	Procedure site - Direct (attribute)	True	Tooth structure	Inferred relationship	Some	1
Electric dental pulp vitality test (procedure)	Procedure site - Direct (attribute)	True	Tooth structure	Inferred relationship	Some	1
Cold dental pulp vitality test	Procedure site - Direct (attribute)	True	Tooth structure	Inferred relationship	Some	1
Hot dental pulp vitality test	Procedure site - Direct (attribute)	True	Tooth structure	Inferred relationship	Some	1
Ethyl chloride dental pulp vitality test	Procedure site - Direct (attribute)	True	Tooth structure	Inferred relationship	Some	1

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

Anatomy structure and entire association reference set (foundation metadata concept)

Anatomy structure and part association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
63923012	Tooth	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
488769012	Tooth structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
771945011	Tooth structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2676771000005115	Tand	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)