FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

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
352112017 Developmental absence of tooth en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
352112017 Developmental absence of tooth en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
623336011 Developmental absence of tooth en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2745236010 Developmental absence of tooth (disorder) en Fully specified name Active Only initial character 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
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
absence de développement d'une dent Is a Hereditary disorder of tooth true Inferred relationship Existential restriction modifier (core metadata concept)
absence de développement d'une dent Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
absence de développement d'une dent Finding site Tooth structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
absence de développement d'une dent Associated morphology Absence (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
absence de développement d'une dent Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
absence de développement d'une dent Is a Malformation of tooth true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group
Familial hypodontia Is a True absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
Hypodontia and nail dysgenesis Is a True absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
Anodontia Is a True absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
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 absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
Oligodontia and cancer predisposition syndrome Is a True absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
Epidermolysis bullosa simplex with hypodontia Is a True absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) Is a False absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
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 absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
X-linked hypodontia (disorder) Is a True absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
X-linked oligodontia (disorder) Is a True absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
Agenesis of enamel Is a True absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
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 absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)
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 absence de développement d'une dent Inferred relationship Existential restriction modifier (core metadata concept)

Reference Sets

Concept inactivation indicator attribute value reference set (foundation metadata concept)

SAME AS association reference set (foundation metadata concept)

Back to Start