FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

26597004: Enamel hypoplasia (disorder)

Status: current, 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
44531012 Enamel hypoplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
757047012 Enamel hypoplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5919981000241114 hypoplasie de l'émail fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

18 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Enamel hypoplasia Is a Disease of teeth false Inferred relationship Some
Enamel hypoplasia Is a Disorder of teeth AND/OR supporting structures (disorder) false Inferred relationship Some
Enamel hypoplasia Finding site Enamel structure false Inferred relationship Some 1
Enamel hypoplasia Associated morphology Hypoplasia false Inferred relationship Some 1
Enamel hypoplasia Finding site Jaw region structure false Inferred relationship Some
Enamel hypoplasia Is a Disorder of hard tissues of teeth (disorder) true Inferred relationship Some
Enamel hypoplasia Associated morphology Hypoplasia true Inferred relationship Some 1
Enamel hypoplasia Finding site Enamel structure true Inferred relationship Some 1
Enamel hypoplasia Is a Oral lesion false Inferred relationship Some
Enamel hypoplasia Is a Developmental anomaly of tooth false Inferred relationship Some
Enamel hypoplasia Is a Hypoplasia of tooth (disorder) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Generalized enamel hypoplasia of undetermined etiology Is a True Enamel hypoplasia Inferred relationship Some
Generalized enamel hypoplasia associated with systemic disease Is a True Enamel hypoplasia Inferred relationship Some
Generalized enamel hypoplasia associated with radiation therapy Is a True Enamel hypoplasia Inferred relationship Some
Generalized enamel hypoplasia associated with ingestion of drugs Is a True Enamel hypoplasia Inferred relationship Some
Localised enamel hypoplasia of undetermined aetiology Is a False Enamel hypoplasia Inferred relationship Some
Localized enamel hypoplasia associated with localized trauma Is a False Enamel hypoplasia Inferred relationship Some
Localized enamel hypoplasia associated with local infection Is a False Enamel hypoplasia Inferred relationship Some
Amelogenesis imperfecta Is a False Enamel hypoplasia Inferred relationship Some
Antenatal enamel hypoplasia Is a True Enamel hypoplasia Inferred relationship Some
Neonatal enamel hypoplasia Is a True Enamel hypoplasia Inferred relationship Some
Dental caries associated with enamel hypoplasia Associated with True Enamel hypoplasia Inferred relationship Some 2
Turner's tooth Is a True Enamel hypoplasia Inferred relationship Some
Hypoplasia of enamel due to congenital syphilis Is a True Enamel hypoplasia Inferred relationship Some
Localized enamel hypoplasia (disorder) Is a True Enamel hypoplasia Inferred relationship Some
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. Is a True Enamel hypoplasia Inferred relationship Some
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. Is a True Enamel hypoplasia Inferred relationship Some
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. Is a True Enamel hypoplasia Inferred relationship Some
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. Is a True Enamel hypoplasia Inferred relationship Some
Generalized enamel hypoplasia associated with fluorosis Is a True Enamel hypoplasia Inferred relationship Some
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. Is a True Enamel hypoplasia Inferred relationship Some

This concept is not in any reference sets

Back to Start