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770944002: syndrome oculo-oto-dentaire (trouble)

SNOMED CT Concept\constatation clinique\...

\Digestive system finding (finding)\Finding of mouth region (finding)\maladie de la cavité buccale\Disorder of teeth AND/OR supporting structures (disorder)\Tooth disorder\Disorder of tooth development (disorder)\Malformation of tooth (disorder)\Macrodontia\Globodontia (disorder)\Oculootodental syndrome
\Digestive system finding (finding)\Finding of mouth region (finding)\Oral cavity finding\Tooth finding\Tooth disorder\Disorder of tooth development (disorder)\Malformation of tooth (disorder)\Macrodontia\Globodontia (disorder)\Oculootodental syndrome
\Digestive system finding (finding)\Finding of mouth region (finding)\Oral cavity finding\Disorder of teeth AND/OR supporting structures (disorder)\Tooth disorder\Disorder of tooth development (disorder)\Malformation of tooth (disorder)\Macrodontia\Globodontia (disorder)\Oculootodental syndrome
\Digestive system finding (finding)\maladie de l'appareil digestif\Disorder of digestive tract (disorder)\Disorder of upper digestive tract (disorder)\maladie de la cavité buccale\Disorder of teeth AND/OR supporting structures (disorder)\Tooth disorder\Disorder of tooth development (disorder)\Malformation of tooth (disorder)\Macrodontia\Globodontia (disorder)\Oculootodental syndrome
\Digestive system finding (finding)\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\Tooth disorder\Disorder of tooth development (disorder)\Malformation of tooth (disorder)\Macrodontia\Globodontia (disorder)\Oculootodental syndrome

\constatation à propos de l'oreille et de l'audition\affection du système auditif\Hearing disorder\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Oculootodental syndrome
\constatation à propos de l'oreille et de l'audition\affection du système auditif\Hearing disorder\perte auditive (trouble)\Hearing loss associated with syndrome\Oculootodental syndrome
\constatation à propos de l'oreille et de l'audition\affection du système auditif\Hearing disorder\perte auditive (trouble)\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Oculootodental syndrome
\constatation à propos de l'oreille et de l'audition\affection du système auditif\affection de l'oreille\Oculootodental syndrome
\constatation à propos de l'oreille et de l'audition\Ear finding\affection de l'oreille\Oculootodental syndrome
\constatation à propos de l'oreille et de l'audition\constatation sur l'audition\Hearing disorder\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Oculootodental syndrome
\constatation à propos de l'oreille et de l'audition\constatation sur l'audition\Hearing disorder\perte auditive (trouble)\Hearing loss associated with syndrome\Oculootodental syndrome
\constatation à propos de l'oreille et de l'audition\constatation sur l'audition\Hearing disorder\perte auditive (trouble)\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Oculootodental syndrome

\constatation fonctionnelle\constatation sur l'audition\Hearing disorder\...

\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Oculootodental syndrome

\perte auditive (trouble)\Hearing loss associated with syndrome\Oculootodental syndrome
\perte auditive (trouble)\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Oculootodental syndrome

\Disease\anomalie chromosomique\maladie chromosomique congénitale\Anomaly of chromosome pair\Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 11 (disorder)\Oculootodental syndrome
\Disease\anomalie chromosomique\maladie chromosomique congénitale\Anomaly of chromosome pair\Anomaly of chromosome pair 11\Deletion of part of chromosome 11 (disorder)\Oculootodental syndrome
\Disease\affection d'un système corporel\affection du système auditif\Hearing disorder\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Oculootodental syndrome
\Disease\affection d'un système corporel\affection du système auditif\Hearing disorder\perte auditive (trouble)\Hearing loss associated with syndrome\Oculootodental syndrome
\Disease\affection d'un système corporel\affection du système auditif\Hearing disorder\perte auditive (trouble)\Sensorineural hearing loss\Congenital sensorineural hearing loss (disorder)\Oculootodental syndrome
\Disease\affection d'un système corporel\affection du système auditif\affection de l'oreille\Oculootodental syndrome
\Disease\affection d'un système corporel\maladie de l'appareil digestif\Disorder of digestive tract (disorder)\Disorder of upper digestive tract (disorder)\maladie de la cavité buccale\Disorder of teeth AND/OR supporting structures (disorder)\Tooth disorder\Disorder of tooth development (disorder)\Malformation of tooth (disorder)\Macrodontia\Globodontia (disorder)\Oculootodental syndrome
\Disease\affection d'un système corporel\maladie de l'appareil digestif\Disorder of digestive organ (disorder)\Tooth disorder\Disorder of tooth development (disorder)\Malformation of tooth (disorder)\Macrodontia\Globodontia (disorder)\Oculootodental syndrome
\Disease\Ear, nose and throat disorder\affection de l'oreille\Oculootodental syndrome
\Disease\affection de la tête\maladie de la cavité buccale\Disorder of teeth AND/OR supporting structures (disorder)\Tooth disorder\Disorder of tooth development (disorder)\Malformation of tooth (disorder)\Macrodontia\Globodontia (disorder)\Oculootodental syndrome
\Disease\affection de la tête\affection de la mâchoire\Disorder of teeth AND/OR supporting structures (disorder)\Tooth disorder\Disorder of tooth development (disorder)\Malformation of tooth (disorder)\Macrodontia\Globodontia (disorder)\Oculootodental syndrome
\Disease\affection de la tête\affection de l'oreille\Oculootodental syndrome
\Disease\Congenital disease\Congenital malformation\Oculootodental syndrome
\Disease\Congenital disease\Congenital hearing disorder\Congenital sensorineural hearing loss (disorder)\Oculootodental syndrome
\Disease\Congenital disease\maladie chromosomique congénitale\Anomaly of chromosome pair\Monosomy and deletion from autosome\Deletion of part of autosome\Deletion of part of chromosome 11 (disorder)\Oculootodental syndrome
\Disease\Congenital disease\maladie chromosomique congénitale\Anomaly of chromosome pair\Anomaly of chromosome pair 11\Deletion of part of chromosome 11 (disorder)\Oculootodental syndrome
\Disease\trouble du développement\Disorder of tooth development (disorder)\Malformation of tooth (disorder)\Macrodontia\Globodontia (disorder)\Oculootodental syndrome
\Disease\trouble du développement\Congenital malformation\Oculootodental syndrome

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

Descriptions:

Id Description Lang Type Status Case? Module

1015831000172119 syndrome OOD (oculo-oto-dentaire) fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

3703553016 Oculootodental syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3703555011 Oculootodental syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

770071000241116 syndrome oculo-oto-dentaire (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

976171000172117 syndrome oculo-oto-dentaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

3703554010 A contiguous gene syndrome comprising otodental syndrome (globodontia and sensorineural high-frequency hearing deficit) associated with eye abnormalities typically including iris and chorioretinal coloboma and sometimes microcornea, microphthalmos, lenticular opacity, lens coloboma and iris pigment epithelial atrophy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Oculootodental syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Oculootodental syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	3
Oculootodental syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	2
Oculootodental syndrome	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	4
Oculootodental syndrome	morphologie associée (attribut)	Enlargement (morphologic abnormality)	true	Inferred relationship	Some	4
Oculootodental syndrome	est un(e) (attribut)	affection de l'oreille	true	Inferred relationship	Some
Oculootodental syndrome	morphologie associée (attribut)	Developmental abnormality	false	Inferred relationship	Some	6
Oculootodental syndrome	localisation d'une constatation (attribut)	dent (structure corporelle)	false	Inferred relationship	Some	6
Oculootodental syndrome	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	6
Oculootodental syndrome	est un(e) (attribut)	Congenital malformation	true	Inferred relationship	Some
Oculootodental syndrome	survenue (attribut)	congénital	true	Inferred relationship	Some	2
Oculootodental syndrome	morphologie associée (attribut)	Partial monosomy (morphologic abnormality)	true	Inferred relationship	Some	1
Oculootodental syndrome	est un(e) (attribut)	Globodontia (disorder)	true	Inferred relationship	Some
Oculootodental syndrome	survenue (attribut)	congénital	true	Inferred relationship	Some	3
Oculootodental syndrome	est un(e) (attribut)	Congenital sensorineural hearing loss (disorder)	true	Inferred relationship	Some
Oculootodental syndrome	localisation d'une constatation (attribut)	Chromosome pair 11 (cell structure)	true	Inferred relationship	Some	1
Oculootodental syndrome	est un(e) (attribut)	Hearing loss associated with syndrome	true	Inferred relationship	Some
Oculootodental syndrome	survenue (attribut)	congénital	false	Inferred relationship	Some	4
Oculootodental syndrome	localisation d'une constatation (attribut)	Long arm of chromosome (cell structure)	true	Inferred relationship	Some	2
Oculootodental syndrome	morphologie associée (attribut)	Partial monosomy (morphologic abnormality)	true	Inferred relationship	Some	2
Oculootodental syndrome	survenue (attribut)	congénital	true	Inferred relationship	Some	1
Oculootodental syndrome	interprète (attribut)	Hearing, function (observable entity)	true	Inferred relationship	Some	5
Oculootodental syndrome	est un(e) (attribut)	Deletion of part of chromosome 11 (disorder)	true	Inferred relationship	Some
Oculootodental syndrome	morphologie associée (attribut)	Congenital enlargement (morphologic abnormality)	false	Inferred relationship	Some	4
Oculootodental syndrome	localisation d'une constatation (attribut)	oreille	true	Inferred relationship	Some	3
Oculootodental syndrome	localisation d'une constatation (attribut)	dent (structure corporelle)	true	Inferred relationship	Some	4

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
1015831000172119	syndrome OOD (oculo-oto-dentaire)	fr	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3703553016	Oculootodental syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3703555011	Oculootodental syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
770071000241116	syndrome oculo-oto-dentaire (trouble)	fr	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
976171000172117	syndrome oculo-oto-dentaire	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Common French translation module (core metadata concept)
3703554010	A contiguous gene syndrome comprising otodental syndrome (globodontia and sensorineural high-frequency hearing deficit) associated with eye abnormalities typically including iris and chorioretinal coloboma and sometimes microcornea, microphthalmos, lenticular opacity, lens coloboma and iris pigment epithelial atrophy.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core