716180009: Odontoma dysphagia syndrome (disorder)

SNOMED CT Concept\Clinical finding (finding)\...

\Digestive system finding (finding)\Disorder of digestive system (disorder)\...

\Digestive system hereditary disorder (disorder)\Odontoma dysphagia syndrome (disorder)

\Disorder of digestive tract (disorder)\Disorder of upper digestive tract (disorder)\Dysphagia\Odontoma dysphagia syndrome (disorder)

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder (disorder)\Odontoma dysphagia syndrome (disorder)
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Odontoma dysphagia syndrome (disorder)
\Disease\Neoplasm and/or hamartoma (disorder)\Neoplastic disease\Benign neoplastic disease\Odontoma dysphagia syndrome (disorder)
\Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder (disorder)\Odontoma dysphagia syndrome (disorder)
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Digestive system hereditary disorder (disorder)\Odontoma dysphagia syndrome (disorder)
\Disease\Disorder of body system\Disorder of digestive system (disorder)\Disorder of digestive tract (disorder)\Disorder of upper digestive tract (disorder)\Dysphagia\Odontoma dysphagia syndrome (disorder)
\Disease\Congenital disease (disorder)\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Odontoma dysphagia syndrome (disorder)
\Disease\Developmental disorder\Developmental hereditary disorder\Odontoma dysphagia syndrome (disorder)
\Disease\Developmental disorder\Congenital malformation\Congenital malformation syndrome (disorder)\Multiple system malformation syndrome\Odontoma dysphagia syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

3304990013 Odontoma dysphagia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

3304991012 Odontoma dysphagia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3304992017 Boder syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

3304993010 Odontoma-dysphagia syndrome is a malformation syndrome, with characteristics of odontomas and severe dysphagia. Less than ten cases have been reported so far. Three of the reported patients manifested multiple odontomas. Occasionally, cardiac, renal and hepatic involvement has been described. In several cases, autosomal dominant inheritance has been suspected. Currently, there are no genes associated with this condition. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core

4769131000172119 syndroom van odontomatose en stenose van aorta en oesofagus nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

4769141000172114 syndroom van odontomen en dysfagie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

4769151000172111 syndroom van Bader nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

4769161000172113 syndroom van Boder nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Odontoma dysphagia syndrome (disorder)	Is a	Dysphagia	true	Inferred relationship	Some
Odontoma dysphagia syndrome (disorder)	Is a	Multiple system malformation syndrome	true	Inferred relationship	Some
Odontoma dysphagia syndrome (disorder)	Is a	Digestive system hereditary disorder (disorder)	true	Inferred relationship	Some
Odontoma dysphagia syndrome (disorder)	Finding site	Upper digestive tract structure	true	Inferred relationship	Some	2
Odontoma dysphagia syndrome (disorder)	Interprets	Functional observable	false	Inferred relationship	Some
Odontoma dysphagia syndrome (disorder)	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	3
Odontoma dysphagia syndrome (disorder)	Occurrence	Congenital	false	Inferred relationship	Some	3
Odontoma dysphagia syndrome (disorder)	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	true	Inferred relationship	Some	1
Odontoma dysphagia syndrome (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1
Odontoma dysphagia syndrome (disorder)	Pathological process (attribute)	Pathological developmental process	true	Inferred relationship	Some	1
Odontoma dysphagia syndrome (disorder)	Interprets	Function (observable entity)	false	Inferred relationship	Some	3
Odontoma dysphagia syndrome (disorder)	Is a	Developmental hereditary disorder	true	Inferred relationship	Some
Odontoma dysphagia syndrome (disorder)	Associated morphology	Benign odontoma	true	Inferred relationship	Some	3
Odontoma dysphagia syndrome (disorder)	Is a	Benign neoplastic disease	true	Inferred relationship	Some

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
3304990013	Odontoma dysphagia syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3304991012	Odontoma dysphagia syndrome	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
3304992017	Boder syndrome	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
3304993010	Odontoma-dysphagia syndrome is a malformation syndrome, with characteristics of odontomas and severe dysphagia. Less than ten cases have been reported so far. Three of the reported patients manifested multiple odontomas. Occasionally, cardiac, renal and hepatic involvement has been described. In several cases, autosomal dominant inheritance has been suspected. Currently, there are no genes associated with this condition.	en	Definition	Active	Entire term case sensitive (core metadata concept)	SNOMED CT core
4769131000172119	syndroom van odontomatose en stenose van aorta en oesofagus	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4769141000172114	syndroom van odontomen en dysfagie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
4769151000172111	syndroom van Bader	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)
4769161000172113	syndroom van Boder	nl	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	Belgian module (core metadata concept)