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

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)

Back to Start

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