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76993005: Enamel structure (body structure)


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
127815013 Enamel en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
503430010 Enamel structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
817774016 Enamel structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


17 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Enamel structure Is a Structure of crown of tooth true Inferred relationship Some
Enamel structure partie de Entire crown of tooth false Additional relationship Some
Enamel structure Laterality Side (qualifier value) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Secondary non-active dental caries extending into enamel (disorder) Finding site True Enamel structure Inferred relationship Some 1
Acquired discoloration of enamel Finding site True Enamel structure Inferred relationship Some 2
Acquired discoloration of enamel associated with aging Finding site True Enamel structure Inferred relationship Some 1
Extensive stage caries of crown of tooth (disorder) Finding site True Enamel structure Inferred relationship Some 1
Initial stage active caries of crown of tooth (disorder) Finding site True Enamel structure Inferred relationship Some 1
Initial stage active caries of crown of tooth (disorder) Finding site True Enamel structure Inferred relationship Some 2
Initial stage non-active caries of crown of tooth (disorder) Finding site True Enamel structure Inferred relationship Some 1
Moderate stage coronal caries Finding site True Enamel structure Inferred relationship Some 1
Moderate stage non-active coronal caries Finding site True Enamel structure Inferred relationship Some 1
Extensive stage non-active caries of crown of tooth (disorder) Finding site True Enamel structure Inferred relationship Some 1
Moderate stage active coronal caries Finding site True Enamel structure Inferred relationship Some 1
Extensive stage active caries of crown of tooth (disorder) Finding site True Enamel structure Inferred relationship Some 1
Initial stage non-active caries of crown of tooth (disorder) Finding site True Enamel structure Inferred relationship Some 2
Initial stage coronal caries Finding site True Enamel structure Inferred relationship Some 1
Initial stage coronal caries Finding site True Enamel structure Inferred relationship Some 2
Stimmler syndrome is characterized by the association of microcephaly, low birth weight and severe intellectual deficit with dwarfism, small teeth and diabetes mellitus. Two cases have been described. Biochemical tests reveal the presence of high levels of alanine in the urine and elevated alanine, pyruvate and lactate levels in the blood. Finding site True Enamel structure Inferred relationship Some 2
Pfeiffer-Palm-Teller syndrome is a very rare dysmorphic syndrome described in two siblings and characterised by a short stature, unique facies, enamel hypoplasia, progressive joint stiffness, high-pitched voice, cup-shaped ears, and narrow palpebral fissures with epicanthal folds, and intellectual deficit. Finding site True Enamel structure Inferred relationship Some 1
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 Enamel structure Inferred relationship Some 1
Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome is a rare, genetic, syndromic intellectual disability disorder characterised by severe intellectual disability with significant speech and language impairment, hypohidrosis (often resulting in hyperthermia) with normal sweat gland appearance, tooth enamel hypoplasia, palmoplantar hyperkeratosis and a high frequency of acquired microcephaly. Mild facial dysmorphism, including lateral flaring of the eyebrows, broad nasal tip, and thick vermilion border, may also be observed. Finding site True Enamel structure Inferred relationship Some 2
A rare junctional epidermolysis bullosa subtype characterized by late-onset blistering surrounded by erythema and localized on the anterior aspect of the lower legs, associated with dystrophic toenails, tooth enamel defects and mild to severe intellectual disability. Lens subluxation and mild facial dysmorphism (with short midface, prognathism and thin upper lip vermilion) are additional reported features. There have been no further descriptions in the literature since 1992. Finding site True Enamel structure Inferred relationship Some 1
Abrasion of tooth extending into pulp (disorder) Finding site True Enamel structure Inferred relationship Some 1
Friction injury of tooth extending into dentine (disorder) Finding site True Enamel structure Inferred relationship Some 2
Friction injury of tooth extending into pulp (disorder) Finding site True Enamel structure Inferred relationship Some 3
Abrasion of tooth extending into dentine (disorder) Finding site True Enamel structure Inferred relationship Some 1
Associates gingival fibromatosis with dental abnormalities including generalized thin hypoplastic amelogenesis imperfecta, intrapulpal calcifications and delay of tooth eruption. Finding site True Enamel structure Inferred relationship Some 2
A rare ectodermal dysplasia syndrome characterized by the association of amelogenesis imperfecta and trichodysplasia with symmetrical pits in the cuticles of hair shafts. There have been no further descriptions in the literature since 1993. Finding site True Enamel structure Inferred relationship Some 2
An exceedingly rare form of brachyolmia, characterized by mild platyspondyly, broad ilia, elongated femoral necks with coxa valga, scoliosis, and short trunked short stature associated with amelogenesis imperfecta of both primary and permanent dentition. Finding site True Enamel structure Inferred relationship Some 4
Amelogenesis imperfecta co-occurrent with cone rod dystrophy Finding site True Enamel structure Inferred relationship Some 1
Enamel-renal syndrome Finding site True Enamel structure Inferred relationship Some 3
Enamel and dentine fracture (disorder) Finding site True Enamel structure Inferred relationship Some 1
Erythrokeratodermia-cardiomyopathy syndrome is a rare, genetic erythrokeratoderma disorder characterized by generalized cutaneous erythema with fine white scales and pruritus refractory to treatment, progressive dilated cardiomyopathy, palmoplantar keratoderma, sparse or absent eyebrows and eyelashes, sparse scalp hair, nail dystrophy, and dental enamel anomalies. Variable features include failure to thrive, developmental delay, and development of corneal opacities. Histology shows psoriasiform acanthosis, hypogranulosis, and compact orthohyperkeratosis. Finding site True Enamel structure Inferred relationship Some 3
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 True Enamel structure Inferred relationship Some 6
Hypomineralisation of enamel of second primary molar tooth Finding site False Enamel structure Inferred relationship Some 1
Hypomineralization of enamel of teeth Finding site True Enamel structure Inferred relationship Some 1
Fixation of orthodontic bracket to enamel of tooth using bonding agent (procedure) Procedure site - Indirect (attribute) True Enamel structure Inferred relationship Some 1
A rare ectodermal dysplasia syndrome characterized by hypotrichosis, tooth enamel hypoplasia, hypoplastic nails, palmoplantar keratoderma, hyperhidrosis on hands, face, and scalp, bilateral partial cutaneous syndactyly, and dysmorphic facial features with large prominent ear pinnae, pointed nose, and thin upper lips. Association of cardiomegaly has also been reported. Finding site True Enamel structure Inferred relationship Some 6
Structure of enamel of molar tooth (body structure) Is a True Enamel structure Inferred relationship Some
Structure of enamel of incisor tooth (body structure) Is a True Enamel structure Inferred relationship Some

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Reference Sets

Lateralizable body structure reference set (foundation metadata concept)

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

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