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234951001: Developmental absence of tooth (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
352112017 Developmental absence of tooth en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2745236010 Developmental absence of tooth (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6071781000241113 absence de développement dentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6071791000241110 absence de développement d'une dent fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


14 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Developmental absence of tooth Is a Hereditary disorder of tooth true Inferred relationship Some
Developmental absence of tooth Is a Developmental hereditary disorder true Inferred relationship Some
Developmental absence of tooth Finding site Tooth structure true Inferred relationship Some 1
Developmental absence of tooth Associated morphology Absence (morphologic abnormality) true Inferred relationship Some 1
Developmental absence of tooth Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Developmental absence of tooth Is a Malformation of tooth (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial hypodontia Is a True Developmental absence of tooth Inferred relationship Some
Hypodontia and nail dysgenesis Is a True Developmental absence of tooth Inferred relationship Some
Anodontia Is a True Developmental absence of tooth 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 Developmental absence of tooth 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 Developmental absence of tooth Inferred relationship Some
Epidermolysis bullosa simplex with hypodontia Is a True Developmental absence of tooth Inferred relationship Some
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) Is a False Developmental absence of tooth 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 Developmental absence of tooth Inferred relationship Some
X-linked hypodontia (disorder) Is a True Developmental absence of tooth Inferred relationship Some
X-linked oligodontia (disorder) Is a True Developmental absence of tooth Inferred relationship Some
A form of amelogenesis imperfecta characterized by incomplete formation of the dental enamel and transmitted as an X-linked or autosomal dominant trait. Is a True Developmental absence of tooth 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 Developmental absence of tooth Inferred relationship Some
This syndrome has characteristics of congenital absence of the teeth and sparse or absent hair. Taurodontia is also present in the majority of cases. The syndrome has been described in less than 15 patients from different families. Is a True Developmental absence of tooth Inferred relationship Some

This concept is not in any reference sets

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