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787414001: Oligodontia (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5408790010 Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5408791014 Oligodontia is a rare developmental dental anomaly in humans characterised by the absence of six or more teeth. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3775387016 Oligodontia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3775388014 Selective tooth agenesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3775389018 Oligodontia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
926401000195111 oligodontia it Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7668941000241114 agénésie dentaire sélective fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
7668951000241112 oligodontie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3395501001000116 Oligodontie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Occurrence Congenital true Inferred relationship Some 2
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Occurrence Congenital true Inferred relationship Some 1
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Finding site Entire tooth false Inferred relationship Some 2
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Finding site Entire tooth false Inferred relationship Some 1
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Is a Partial congenital absence of teeth true Inferred relationship Some
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Associated morphology Congenital abnormal number false Inferred relationship Some 2
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Associated morphology Congenital absence false Inferred relationship Some 1
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 1
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Finding site Dentition true Inferred relationship Some 1
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Finding site Tooth structure true Inferred relationship Some 2
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Is a Congenital absence of jaw true Inferred relationship Some
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Is a Congenital absence of mouth true Inferred relationship Some
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Is a Malformation of teeth (disorder) true Inferred relationship Some
Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Associated morphology Abnormal number (morphologic abnormality) true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
X-linked oligodontia (disorder) Is a True Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Inferred relationship Some
Spondyloepimetaphyseal dysplasia-abnormal dentition syndrome is a rare primary bone dysplasia disorder characterized by the association of dental anomalies (oligodontia with pointed incisors) and generalized platyspondyly with epiphyseal and metaphyseal involvement. Thin tapering fingers and accentuated palmar creases are additional features. Is a True Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Inferred relationship Some
A rare, genetic, odontologic disease characterized by congenital absence of six or more permanent teeth (excluding the third molars) in association with an increased risk for malignancies, ranging from gastrointestinal polyposis to early-onset colorectal cancer and/or breast cancer. Ectodermal dysplasia (manifesting with sparse hair and/or eyebrows) may also be associated. Is a True Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Inferred relationship Some
A rare congenital malformation syndrome characterized by cleft soft palate, severe oligodontia of the deciduous teeth, absence of the permanent dentition, bilateral conductive deafness due to fixation of the footplate of the stapes, short halluces with a wide space between the first and second toes, and fusion of carpal and tarsal bones. There have been no further descriptions in the literature since 1971. Is a True Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Inferred relationship Some
Deafness-oligodontia syndrome is characterized by sensorineural hearing loss and oligodontia/hypodontia. It has been described in two pairs of siblings and in one isolated case. Dizziness was reported in one of the pairs of siblings. Transmission appears to be autosomal recessive. Is a True Oligodontia is a rare developmental dental anomaly in humans characterized by the absence of six or more teeth. Inferred relationship Some

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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