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707310009: Globodontia (disorder)


Status: current, Not 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
3029697017 Globodontia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3029807014 Globodontia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
6305461000241115 globodontie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


2 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Globodontia (disorder) Is a Developmental abnormality of tooth size and form false Inferred relationship Some
Globodontia (disorder) Is a Congenital anomaly of tooth (disorder) false Inferred relationship Some
Globodontia (disorder) Associated morphology anomalie du développement false Inferred relationship Some 2
Globodontia (disorder) Occurrence Congenital false Inferred relationship Some 2
Globodontia (disorder) Finding site Tooth structure false Inferred relationship Some 2
Globodontia (disorder) Finding site Tooth structure true Inferred relationship Some 1
Globodontia (disorder) Occurrence Congenital false Inferred relationship Some 1
Globodontia (disorder) Associated morphology Congenital enlargement false Inferred relationship Some 1
Globodontia (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Globodontia (disorder) Associated morphology Enlargement (morphologic abnormality) true Inferred relationship Some 1
Globodontia (disorder) Is a Macrodontia true Inferred relationship Some
Globodontia (disorder) Pathological process (attribute) Pathological developmental process false Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
A contiguous gene syndrome comprising otodental syndrome (characterized by globodontia and sensorineural high-frequency hearing deficit) associated with eye abnormalities including, typically, iris and chorioretinal coloboma, as well as, on occasion, microcornea, microphthalmos, lenticular opacity, lens coloboma and iris pigment epithelial atrophy. Is a True Globodontia (disorder) Inferred relationship Some
Otodental syndrome is a very rare inherited condition characterized by grossly enlarged canine and molar teeth (globodontia) associated with sensorineural hearing loss. Is a True Globodontia (disorder) Inferred relationship Some

This concept is not in any reference sets

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