716180009: Odontoma dysphagia syndrome (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Digestive system finding\Disorder of digestive system\...
• \Digestive system hereditary disorder\Boder syndrome
• \Disorder of digestive tract\Disorder of upper digestive tract\Dysphagia\Boder syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Boder syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Boder syndrome
• \Disease\Neoplasm and/or hamartoma\Neoplastic disease\Benign neoplastic disease\Boder syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Boder syndrome
• \Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Boder syndrome
• \Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive tract\Disorder of upper digestive tract\Dysphagia\Boder syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Boder syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Boder syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Boder syndrome

Status: current, Primitive. 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	Case insensitive	SNOMED CT core
3304991012	Odontoma dysphagia syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3304992017	Boder syndrome	en	Synonym	Active	Case sensitive	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	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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